72 Political Science jobs in Malaysia

**Job Description**
**Are You Ready to Make It Happen at Mondelēz International?**
**Join our Mission to Lead the Future of Snacking. Make It Matter.**
In this role, you will plan and execute critical pieces of global public and government affairs priorities to advocate for Mondelēz International's interests and implement related transactions or communications with the public and government officials. You are the lead external liaison for key stakeholders and coordinate communications with a wide range of internal and external stakeholders.
**How you will contribute**
As the primary public affairs lead in a market or category, you will drive a proactive government affairs and community involvement agenda, participate in trade associations by assuming leadership positions and participating in executive briefings, and drive sustainable and mindful snacking priorities. In addition, you will advocate on issues important to company, particularly focused on the well-being and sustainability agenda; manage business-critical emerging issues by advocating on behalf of the company; map and assess reputation and business risks and develop an action plan, and ensure that activities are delivered within budget.
**What you will bring**
A desire to lead the future for our company and accelerate you career with experience and knowledge in:
+ Corporate Affairs
+ Business and brands
+ Communication skills-including the ability to coach and advise leaders, and to manage cross-functional teams
+ Risk assessment and scenario planning
+ Influencing others both internally and externally
+ Understanding of the regulatory and consumer environment
+ Creating strong internal and external relationships
No Relocation support available
**Business Unit Summary**
**Mondelēz International in Southeast Asia is in five countries serving 19 markets with more than 18 nationalities and 7,500 employees. This group is emerging as one of the fastest growing regions in Asia, the Middle East and Africa, and we are proud of consistently producing high quality products in nine manufacturing sites. We are market leaders in key snacking categories, making and selling brands like** **_Oreo_** **and** **_Tiger_** **biscuits,** **_Kinh Do_** **mooncakes,** **_Jacob's_** **crackers,** **_Cadbury Dairy Milk_** **chocolate,** **_Tang_** **powdered beverage,** **_Halls_** **candy and** **_Eden_** **cheese. We set the benchmark in being a responsible business and contributing to the communities in which we operate.**
Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
**Job Type**
Regular
Communications and Public & Government Affairs
Corporate & Government Affairs
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about.
We have a rich portfolio of strong brands - both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum
Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast.
Join us and Make It An Opportunity!
Mondelez Global LLC is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants who require accommodation to participate in the job application process may contact for assistance.

Corporate & Government Affairs Lead MYSG page is loaded Corporate & Government Affairs Lead MYSG Apply locations Selangor, Malaysia time type Full time posted on Posted 2 Days Ago job requisition id R-144078 Job Description

Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It Matter. In this role, you will plan and execute critical pieces of global public and government affairs priorities to advocate for Mondelēz International’s interests and implement related transactions or communications with the public and government officials. You are the lead external liaison for key stakeholders and coordinate communications with a wide range of internal and external stakeholders. How you will contribute As the primary public affairs lead in a market or category, you will drive a proactive government affairs and community involvement agenda, participate in trade associations by assuming leadership positions and participating in executive briefings, and drive sustainable and mindful snacking priorities. In addition, you will advocate on issues important to company, particularly focused on the well-being and sustainability agenda; manage business-critical emerging issues by advocating on behalf of the company; map and assess reputation and business risks and develop an action plan, and ensure that activities are delivered within budget. What you will bring A desire to lead the future for our company and accelerate you career with experience and knowledge in: Corporate Affairs Business and brands Communication skills—including the ability to coach and advise leaders, and to manage cross-functional teams Risk assessment and scenario planning Influencing others both internally and externally Understanding of the regulatory and consumer environment Creating strong internal and external relationships No Relocation support available

Business Unit Summary

Mondelēz International in Southeast Asia is in five countries serving 19 markets with more than 18 nationalities and 7,500 employees. This group is emerging as one of the fastest growing regions in Asia, the Middle East and Africa, and we are proud of consistently producing high quality products in nine manufacturing sites. We are market leaders in key snacking categories, making and selling brands like

Oreo

and

Tiger

biscuits,

Kinh Do

mooncakes,

Jacob’s

crackers,

Cadbury Dairy Milk

chocolate,

Tang

powdered beverage,

Halls

candy and

Eden

cheese. We set the benchmark in being a responsible business and contributing to the communities in which we operate.

Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type

RegularCommunications and Public & Government AffairsCorporate & Government Affairs At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about. We have a rich portfolio of strong brands – both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum Our 80,000 Makers and Bakers are located in our operations in more than80countries and are working to sell our products in over150countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast.

#J-18808-Ljbffr

Section Head, Regulatory Development & Government Affairs

U Mobile Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia

Section Head, Regulatory Development & Government Affairs

U Mobile Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia

Get AI-powered advice on this job and more exclusive features.

Life at U Mobile

We are Passionate, Innovative, Trustworthy, Team-Oriented & Fun-Loving.

Life at U Mobile

We are Passionate, Innovative, Trustworthy, Team-Oriented & Fun-Loving.

At U Mobile, we are always on the lookout for great talents and passionate individuals to join our growing team.

Let’s start your journey with an award-winning organization!

#UnbeatableCareerAwaits

Top Reasons To Join Us!

• Awarded For
• Most Preferred Employers in Telecommunication Industry (2022, 2023 & 2024)
• Bronze Winner in Cross-Generational Workforce Engagement (2024)
• Gold Winner for Excellence in Workplace Culture (2021)
• Comprehensive medical, dental, optical and insurance benefits
• Flexi working hours arrangements
• Staff Line & Device Subsidy
• Smart Casual Attire
• Child Parental Care Leave
• Convenient location with access to public transport (Imbi Monorail/Bukit Bintang MRT)
• Special employee discounts for selected F&B Brands
  
  

Job Summary

Section Head of Regulatory Development & Government Affairs plays a key role in supporting the company’s engagement with regulators and government stakeholders. This role is responsible for monitoring policy developments, preparing company positions, and ensuring effective participation in regulatory consultations and forums. Working under the direction of the GM, this role acts as a regulatory partner to internal teams, ensuring business initiatives align with national regulatory directions and obligations.

The Day-To-Day Activities

Regulatory Development & Policy Monitoring

• Track and interpret developments in telecommunications and digital economy regulations, policies, and public consultations.
• Draft regulatory responses, policy position papers, and briefing materials for internal and external stakeholders.
• Support internal alignment by analyzing implications of proposed regulatory changes and pre-paring impact assessments.
  
  

Government & Stakeholder Engagement

• Represent the company in working-level engagements with regulatory authorities (e.g., MCMC), ministries (e.g., KKD, MITI), and industry groups.
• Coordinate and participate in industry forums, task forces, and regulatory discussions, ensuring company positions are well-articulated.
• Prepare and support senior leadership’s participation in higher-level meetings with government bodies.
  
  

Internal Advisory & Cross-Functional Collaboration

• Work closely with Legal, Product, Technology, Commercial, and Enterprise teams to embed regulatory insights into business plans, product development, and go-to-market activities.
• Provide guidance on licensing, compliance obligations, policy advocacy opportunities, and risk mitigation for new or existing services.
• Consolidate business inputs and translate them into aligned regulatory submissions or positions.
  
  

Submissions & Documentation

• Lead the preparation of accurate, timely, and high-quality regulatory submissions, reports, and correspondence.
• Maintain a structured and auditable record of regulatory filings, key engagement notes, and internal decision making trails.
  
  

About You

• Bachelor’s degree in Law, Public Policy, Business, Economics, Engineering, or a related discipline.
• Additional certifications in regulatory affairs, policy advocacy, or public administration are ad-vantageous.
• 15 years of experience in regulatory affairs, government relations, or public policy, preferably within telco, tech, or a regulated industry.
• Demonstrated experience preparing regulatory submissions, engaging with government stakeholders, and navigating compliance matters.
• Strong understanding of Malaysian telecommunications regulations and policymaking pro-cesses.
• Excellent writing and communication skills — able to translate technical/regulatory matters into clear business advice.
• Stakeholder management — able to build rapport with regulators, internal business units, and industry peers.
• High attention to detail, with strong organizational skills in managing multiple regulatory workstreams.
  
  

What’s Next ? Once you have applied online, our team will review your application and due to a high volume of applications, only shortlisted candidates will be notified.

Seniority level

• Seniority level Executive

Employment type

• Employment type Full-time

Job function

• Job function Business Development and Sales
• Industries Telecommunications

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Government Affairs and Public Policy Manager

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corporate_fare Google place Kuala Lumpur, Federal Territory of Kuala Lumpur, MalaysiaMid

Experience driving progress, solving problems, and mentoring junior team members; with deeper expertise and applied knowledge within relevant areas.

Apply

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• Bachelor's degree or equivalent practical experience.
• 7 years of experience in policy analysis and campaigns, focusing on technology issues or related policy environments.
• 7 years of experience working within government, think tanks, public interest groups, technology industry groups, or corporate public policy organizations.

Preferred qualifications:

• Experience with Internet technologies and related policy environments.
• Ability to stay informed on technical and regulatory issues.
• Interest in the role of the Internet in modern society.
• Excellent communication, presentation, and translation skills.
• Fluency in English and Bahasa Melayu to support regional client relationships.
• Willingness to travel as needed.

About the job

As part of Google’s Government Affairs and Public Policy team, you'll work across regions, product areas, and functions, managing campaigns, projects, and initiatives. Your role involves advocating for Google and bringing external perspectives into the company to shape our policies and strategies. You’ll be passionate about shaping the future of technology use and development for everyone.

Our team engages with government officials, legislators, regulators, and stakeholders to address public policy challenges affecting the internet and beyond, focusing on issues at the intersection of policy, business, and technology.

Responsibilities

• Represent Google in policy-making and government engagements in Malaysia and the Philippines.
• Develop and implement government affairs strategies aligned with Google's objectives in these regions.
• Lead policy campaigns on issues like data privacy, AI ethics, digital economy, content regulation, and competition.
• Build networks with trade associations, industry partners, and other stakeholders to promote an open and user-focused internet.
• Maintain internal communication and provide counsel to teams and leadership.

Google values diversity and is an equal opportunity employer. We are committed to creating a workforce that reflects our users and fostering a culture of belonging. We require English proficiency for all roles to facilitate global collaboration.

Note: Google does not accept unsolicited resumes from recruitment agencies and is not responsible for fees related to such resumes.

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Join to apply for the Research Associate role at Emapta Global

Join to apply for the Research Associate role at Emapta Global

Get AI-powered advice on this job and more exclusive features.

Shape the Future of Legal Expertise Worldwide

Legal expertise crosses borders, and so can your career. In this role, you will research, verify, and connect the right experts with global law firms. While working from Malaysia, you will contribute to cases of international importance and develop skills that set you apart in the legal industry.

What You'll Do

Be part of our client's team as a Research Associate , supporting case management and building a world-class database of experts for litigation. You'll engage in research, expert qualification, and client collaboration while strengthening connections across international legal networks.

Employment type: Full time
Shift: Day Shift
Work setup: Work from Home (Quarterly Onsite Meetings)

Perks and Advantages

• Eight (8) days annual leave
• Diverse and supportive work environment
• Unlimited upskilling through Emapta Academy courses (Want to know more? Visit

What You'll Bring to the Table

• Minimum of 2 years' experience in headhunting or recruitment , preferably in RPO focused on Engineering, Aerospace, Banking, or Insurance C-level roles
• Tertiary education in any discipline
• Strong verbal and written communication skills
• Experience in research, critical thinking, strategy, recruitment, or related fields
• Proven analytical and strategic thinking skills
• Confidence in engaging with diverse professionals via phone and email
• Excellent memory and attention to detail

Your Key Contributions

• Support offshore teams with case management and research assistance
• Research and match the most suitable experts using internal and external resources
• Expand the expert database by onboarding new experts
• Vet, qualify, and conduct background checks on potential experts
• Maintain relationships with offshore teams and subject matter experts
• Manage and grow the database to ensure accurate matching of experts and clients

About the Organization You'll Join

Our client is the leading provider of highly specialized expert witnesses in Australasia. Founded in 2013, they've redefined how lawyers secure expert witnesses for litigation by building a global network of over 10,000 experts across disciplines like engineering, medicine, technology, and commerce. Trusted by more than 2,100 legal firms worldwide, they deliver expert sourcing, case management, quality assurance, and training to ensure optimal outcomes in court. With a mission to streamline the expert witness process, our client continues to revolutionize the legal landscape with innovation and precision.

Who are we?

At Emapta, we believe in building careers that resonate with passion, purpose, and the vibrant spirit of Malaysia. Our diverse roster of over 1,000 international clients spans various industries, offering you a dynamic platform to showcase your skills and make a meaningful impact on a global scale. For over a decade, we have helped companies adapt to ever-changing market needs by providing access to a wide range of talent, office solutions, and more. Our mission is to hone your skills and help you reach the top and become part of the top 1% talent in Malaysia.

Emapta is more than just a company; it's a tight-knit community that values the unique blend of professionalism and Malaysian warmth. Our organization embodies a culture that encourages innovation, collaboration, and continuous learning. Share your passion and enthusiasm across the globe and enjoy the flexibility to thrive in your career while savoring the joys of life outside the office.

Be part of Emapta's story - a story that values diversity, celebrates success, and embraces the colorful culture of Malaysia.

#EmaptaEra

Seniority level

• Seniority level Mid-Senior level

Employment type

• Employment type Full-time

Job function

• Job function Research
• Industries Outsourcing and Offshoring Consulting

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Join to apply for the

Research Associate

role at

Emapta Global Join to apply for the

Research Associate

role at

Emapta Global Get AI-powered advice on this job and more exclusive features. Shape the Future of Legal Expertise Worldwide

Legal expertise crosses borders, and so can your career. In this role, you will research, verify, and connect the right experts with global law firms. While working from Malaysia, you will contribute to cases of international importance and develop skills that set you apart in the legal industry.

What You'll Do

Be part of our client's team as a

Research Associate , supporting case management and building a world-class database of experts for litigation. You'll engage in research, expert qualification, and client collaboration while strengthening connections across international legal networks.

Employment type: Full time Shift: Day Shift Work setup: Work from Home (Quarterly Onsite Meetings)

Perks and Advantages Eight (8) days annual leave Diverse and supportive work environment Unlimited upskilling through Emapta Academy courses (Want to know more? Visit What You'll Bring to the Table Minimum of

2 years' experience in headhunting or recruitment , preferably in RPO focused on Engineering, Aerospace, Banking, or Insurance C-level roles Tertiary education in any discipline Strong verbal and written communication skills Experience in research, critical thinking, strategy, recruitment, or related fields Proven analytical and strategic thinking skills Confidence in engaging with diverse professionals via phone and email Excellent memory and attention to detail Your Key Contributions Support offshore teams with case management and research assistance Research and match the most suitable experts using internal and external resources Expand the expert database by onboarding new experts Vet, qualify, and conduct background checks on potential experts Maintain relationships with offshore teams and subject matter experts Manage and grow the database to ensure accurate matching of experts and clients About the Organization You'll Join

Our client is the leading provider of highly specialized expert witnesses in Australasia. Founded in 2013, they've redefined how lawyers secure expert witnesses for litigation by building a global network of over 10,000 experts across disciplines like engineering, medicine, technology, and commerce. Trusted by more than 2,100 legal firms worldwide, they deliver expert sourcing, case management, quality assurance, and training to ensure optimal outcomes in court. With a mission to streamline the expert witness process, our client continues to revolutionize the legal landscape with innovation and precision.

Who are we?

At Emapta, we believe in building careers that resonate with passion, purpose, and the vibrant spirit of Malaysia. Our diverse roster of over 1,000 international clients spans various industries, offering you a dynamic platform to showcase your skills and make a meaningful impact on a global scale. For over a decade, we have helped companies adapt to ever-changing market needs by providing access to a wide range of talent, office solutions, and more. Our mission is to hone your skills and help you reach the top and become part of the top 1% talent in Malaysia.

Emapta is more than just a company; it's a tight-knit community that values the unique blend of professionalism and Malaysian warmth. Our organization embodies a culture that encourages innovation, collaboration, and continuous learning. Share your passion and enthusiasm across the globe and enjoy the flexibility to thrive in your career while savoring the joys of life outside the office.

Be part of Emapta's story - a story that values diversity, celebrates success, and embraces the colorful culture of Malaysia.

#EmaptaEra Seniority level

Seniority level Mid-Senior level Employment type

Employment type Full-time Job function

Job function Research Industries Outsourcing and Offshoring Consulting Referrals increase your chances of interviewing at Emapta Global by 2x Sign in to set job alerts for “Research Assistant” roles.

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 6 months ago Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 2 weeks ago Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 3 months ago Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 6 months ago Binance Accelerator Program - Research Data Analyst

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Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 week ago Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 week ago Data Partner - Computer Science (Chinese)

Customer Service BI Specialist (Chinese Speaker)

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

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Job Description

Clinical Research Associate (CRA)

• Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR Asia
• We were awarded ‘Sponsor of the Year’ in 2019, 2020, 2022 and 2024 from Clinical Research Malaysia for the highest number of studies and total study value recorded in the country!
• We have a proud legacy of turning breakthrough science into medicines and vaccines that save and improve lives around the world. We are focused on discovering new solutions for today and the future!
• Join the premier biopharmaceutical company that has been in the business for more than 125 years

The role is accountable for performance and compliance for assigned protocols and sites in a country.

Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company’s policies and procedures, quality standards and adverse event reporting requirements internally and externally.

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
Actively develops and expands the territory for clinical research, finding and developing new sites. Participates in internal meetings and workstreams as SME for monitoring processes and systems.

Responsibilities include, but are not limited to:

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
• Participates & provides inputs on site selection and validation activities.
• Performs remote and on-site monitoring & oversight activities using various tools to ensure:
o Data generated at site are complete, accurate and unbiased.
o Subjects’ right, safety and well-being are protected.
• Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
• Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
• Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
• Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA Manager, CRM, TA Head and CRD as needed.
• Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
• Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
• Contributes strongly to CRA team knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.
• Supports and/or leads audit/inspection activities as needed.
• Following the country strategy defined by CRD and CRA manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.
• Mentors / buddies junior CRAs on process/study requirements and performs co-monitoring visits where appropriate.

Extent of Travel:

• Ability to travel domestically and internationally approximately 65%-75% of working time. Expected travelling 2-3 days/week.
• Current driver’s license preferred (Must have in certain countries).

Qualifications, Skills & Experience
CORE Competency Expectations:

• Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively.
• Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
• Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.
• Hands on knowledge of Good Documentation Practices.
• Proven Skills in Site Management including management of site performance and patient recruitment.
• Demonstrated high level of monitoring skill with independent professional judgment.
• Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices.
• Ability to understand and analyse data/metrics and act appropriately.
• Capable of managing complex issues, works in a solution-oriented manner.
• Performs root cause analysis and implements preventative and corrective action.

Behavioural Competency Expectations:

• Effective time management, organizational and interpersonal skills, conflict management, problem solving skills.
• Able to work highly independently across multiple protocols, sites and therapy areas.
• High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.
• Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.
• Demonstrates commitment to Customer focus.
• Works with high quality and compliance mind-set.
• Positive mindset, growth mindset, capable of working independently and being self-driven.
• Demonstrates and projects professional demeanor and communication consistent with organizational policies and practices.

Experience Requirements:
Required:
• Min. 2 years of direct site management (monitoring) experience in a bio/pharma/CRO.

Educational Requirements:
Preferred:
• B.A./B.S. with strong emphasis in science and/or biology.

What we look for …

Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Accountability, Accountability, Adaptability, Adverse Event Reporting System, Biopharmaceutical Industry, Biopharmaceuticals, Clinical Medicine, Clinical Research Methods, Clinical Sciences, Clinical Site Management, Clinical Study Management, Clinical Testing, Clinical Trial Planning, Clinical Trials Monitoring, Data Analysis, Data Reporting, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Healthcare Innovation, Management Process, Medical Research, Monitoring Control, Organizational Performance Management, Problem Solving, Protocol Adherence {+ 4 more}

Preferred Skills:

Job Posting End Date:

07/15/2025

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Requisition ID: R353235

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Tigermed Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia

Clinical Research Associate

Tigermed Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia

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1.1 This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations.

1.2 The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

2.Responsibilities

(a) Site management

•Study site selection, initiation (SIV) and clinical monitoring.

•Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

•Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

•Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

•Track study recruitment to ensure recruitment target is achieved in all studies.

•Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.

•Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

•Assemble site specific EC submission dossier, and ensure submission to EC.

Training

•Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.

•Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

•Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

•Prepare/complete study records’ archiving according to protocol and sponsor requirements.

(b) Drug Safety

•Ensure safety information is disseminated to all sites according SOP and applicable regulations.

•Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

•Finalize budget and obtain signed contract from site, prior to site initiation visit.

•Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

•Update and maintain Study tools/systems in a timely manner.

3. Qualifications

3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. The excellent candidates will not be restricted to the current requirements;

3.2 At least 1 year of CRA experience;

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Seniority level

• Seniority level Associate

Employment type

• Employment type Full-time

Job function

• Job function Research
• Industries Pharmaceutical Manufacturing

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To be an active member of the research team within the Center of Technology, Strategy and Sustainability (CTSS) to be a leading center of excellence and research on business strategies and technology in emerging markets and their socio-political environment. The CTSS hosts a flagship research project and various smaller research projects each year, while actively engaging the academic, policymaking, private sector, and public audiences on the research outputs from the center.

The research associate is an important member in assisting in conducting, publishing, and disseminating rigorous and impactful research. Currently, the CTSS is focusing research on the area of energy transition and renewable energy, including a focus on the energy transition landscape in Malaysia, biomass energy, carbon markets, and other topics.

Key Responsibilities

• To actively assist and perform the research center flagship research project, from planning and initiating research project, literature review, data collection, analysis, writing, and dissemination, in order to ensure the successful publication of research output within the planned period.
• To actively lead, with guidance from the senior members of the research center, in personal research project, from planning and initiating research project, literature review, data collection, analysis, writing, and dissemination, in order to ensure the successful publication of research output within the planned period.
• To assist in organizing and running the research events, workshops, seminars, and events of the research center for the dissemination of the research output and greater engagements between the research centers and the wider research community and public.
• To assist in the research output dissemination to relevant stakeholders from policymakers, private sector stakeholders, civil society stakeholders, and the general public to create research impact from the research project.
• To assist in the general promotion of the research center output and activities to increase awareness of the research center.
• To assist in the engagement with the wider research community globally for the research center to build a wider research network for the research center.
• Participate in the general administrative activities of the center.

Minimum Qualification and Skills Required

• Bachelor Degree in Social Sciences preferred; fresh graduates are welcomed to apply.
• Good command of English and Malay (spoken and written).
• Basic knowledge in research data collection and analysis methodology and tools either in qualitative or quantitative methods.
• Ability to actively learn qualitative and quantitative research data collection and analysis methodology.

Application Process

Interested applicants are urged to submit their resume, cover letter, and any relevant additional documentation.

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