Merck
Job Description
**Associate Clinical Research Associate (ACRA)
**
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 2025 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 135 years.
With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.
Responsibilities include, but are not limited to:
Extent of Travel:
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.
Developing skills in Site Management including management of site performance and patient recruitment.
Developing level of monitoring skill and independent professional judgment.
Good IT skills (Use of MS office, use of some clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices.
Works with high quality and compliance mindset.
Capable of managing complex issues, solution-oriented approach.
Ability to perform root cause analysis and implement preventative and corrective action.
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.
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 and Educational Requirements:
- Associate’s degree, certificate or equivalent in a scientific / healthcare discipline together with at least 3 years of relevant experience in the healthcare field.
Or
- Bachelor’s degree (or above) in a scientific / healthcare discipline together with at least 6months of relevant experience in the healthcare field.
Or
- Bachelor’s degree (or above) in a non-scientific/healthcare discipline together with at least2 years of relevant experience in the healthcare field.
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.
Required Skills:
Accountability, Accountability, Administrative Policies, Adverse Event Report, Biopharmaceutical Industry, Biopharmaceuticals, Clinical Evaluation Reports, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Data Analysis, Early Clinical Development, Finance, Good Clinical Data Management Practice (GCDMP), Investigations Training, IT Change Management, Key Stakeholder Relationships, Pharmacovigilance, Policy Development, Protocol Adherence, Regulatory Affairs Compliance, Regulatory Compliance {+ 1 more}
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
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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):
Job Posting End Date:
09/9/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.