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Clinical Research Associate (CRA) Openings – Pharma Industry
Apply for Clinical Research Associate (CRA) vacancies. B.Sc/M.Sc/Pharmacy graduates with 2–5 years of clinical trial monitoring exp. can apply.
Join one of the world’s leading pharmaceutical companies as a Clinical Research Associate (CRA) and contribute to advancing global healthcare. This role offers the opportunity to oversee and manage clinical trial sites, ensuring strict compliance with ICH-GCP guidelines, local regulations, and company standards. Whether you are looking to grow your career in clinical operations or expand your expertise in trial monitoring, this is a pivotal role in ensuring patient safety and the reliability of clinical data.
Company Overview
Merck & Co., Inc. (also known as Merck Sharp & Dohme LLC) is a global biopharmaceutical leader committed to discovering, developing, and delivering innovative medicines and vaccines. With decades of proven excellence in clinical development, Merck has built a strong reputation for quality, safety, and compliance in its operations worldwide.
Job Role & Responsibilities
As a Clinical Research Associate (CRA), you will:
- Serve as the primary site contact and site manager throughout all study phases.
- Build and maintain strong site relationships, ensuring smooth trial conduct.
- Perform clinical study site management and monitoring in line with ICH-GCP, SOPs, protocols, and monitoring plans.
- Gain in-depth knowledge of study protocols and coordinate tasks for site readiness.
- Conduct site visits including initiation, validation, monitoring, and close-out visits.
- Review regulatory documentation, trial data, and ensure adherence to protocol compliance.
- Monitor data integrity, patient safety, and adherence to quality standards.
- Support site audits, inspections, and CAPA implementation as required.
- Mentor junior CRAs, share best practices, and act as a process Subject Matter Expert (SME).
Eligibility / Qualifications
- Education:
- Associate’s degree or equivalent in healthcare/life sciences + 5 years of relevant experience, including at least 2 years of site monitoring.
- OR Bachelor’s degree (B.Sc, B.Pharm, M.Sc, M.Pharm, Nursing, Biotechnology, or related field) + 2 years of site monitoring experience in pharma/CRO.
- Skills Required:
- Strong knowledge of GCP, ICH guidelines, and country-specific regulations.
- Experience in site management, patient recruitment, and regulatory documentation.
- IT proficiency (MS Office, CTMS, eTMF, and clinical systems).
- Strong problem-solving, time management, and communication skills.
- Ability to analyze clinical data and ensure accurate reporting.
- Behavioral Competencies:
- High accountability, adaptability, and a solution-oriented mindset.
- Effective conflict management and organizational skills.
- Culturally sensitive with ability to work in matrix multicultural environments.
- Demonstrates professionalism, customer focus, and compliance-driven approach.
Location & Work Arrangements
- Regions Covered: Europe, Middle East, Africa, Latin America & Asia Pacific (excluding USA, Canada & Puerto Rico).
- Travel Requirements: Frequent travel to clinical sites as required.
- Work Mode: Flexible working arrangements depending on project needs.
Application Process
Interested candidates can apply directly through the official portal:
Apply Here
Applicants are encouraged to apply before 31st October 2025 to ensure consideration.
Why Join Merck as a CRA?
- Be part of a globally respected pharma leader with a strong focus on innovation.
- Work across diverse therapeutic areas and gain exposure to complex clinical studies.
- Benefit from robust training programs and continuous professional development.
- Collaborate with cross-functional teams in a compliance-driven environment.
- Make a tangible impact on patient safety and global health.
FAQs
Q1. What is the minimum experience required for this role?
At least 2 years of direct clinical trial site monitoring experience in a pharma/CRO is required.
Q2. Can freshers apply for CRA positions at Merck?
This role is not open to freshers. It requires prior hands-on experience in clinical monitoring.
Q3. Is travel mandatory for CRA positions?
Yes, CRAs are required to travel frequently to clinical sites for monitoring visits.
Q4. What qualifications are acceptable?
B.Sc, M.Sc, B.Pharm, M.Pharm, Nursing, Biotechnology, or equivalent healthcare degrees with relevant monitoring experience.
Q5. When is the last date to apply?
The posting is open until 31st October 2025.
Quick Summary Table
| Company | Merck & Co., Inc. (MSD) |
|---|---|
| Vacancies | Clinical Research Associate (CRA) |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm, Nursing, Biotechnology, Life Sciences |
| Experience | 2–5 Years (site monitoring, pharma/CRO) |
| Location | EMEA, Latin America & Asia Pacific (excluding US/Canada) |
| Last Date to Apply | 31st October 2025 |
