MSD Hiring Specialist Clinical Research Associate

MSD Hiring Specialist Clinical Research Associate | Clinical Research Jobs

MSD is hiring experienced professionals for the position of Specialist Clinical Research Associate. This opportunity is ideal for candidates looking to build a long-term career in clinical research, clinical trial monitoring, site management, regulatory compliance, and pharmaceutical research operations.

Candidates with experience in clinical trial management, site monitoring, GCP compliance, pharmacovigilance coordination, and clinical operations can apply for this Clinical Research Associate (CRA) role.

This opening is suitable for professionals from Pharmacy, Life Sciences, Clinical Research, Biotechnology, Biochemistry, Nursing, and allied healthcare backgrounds who want to work in global clinical development programs and regulated pharmaceutical research environments.

The role involves clinical site monitoring, investigator coordination, clinical trial compliance, protocol adherence, safety monitoring, and regulatory documentation management.

Company Overview

MSD, also known globally as Merck & Co., is one of the leading multinational pharmaceutical and healthcare companies focused on developing innovative medicines, vaccines, biologic therapies, and healthcare solutions.

The company operates across several therapeutic areas including:

• Oncology
• Vaccines
• Infectious diseases
• Diabetes
• Cardiovascular healthcare
• Immunology
• Clinical research and development

MSD is recognized for its strong global clinical research infrastructure, ethical research practices, and focus on patient safety and scientific innovation.

Professionals working at MSD gain exposure to:

• Global clinical trials
• Regulatory compliance systems
• Clinical operations management
• Pharmacovigilance activities
• Site monitoring and management
• ICH-GCP compliant research environments
• Clinical data quality systems
• International healthcare research standards

Job Role & Responsibilities

The Specialist Clinical Research Associate will manage and monitor clinical trial sites while ensuring compliance with ICH-GCP guidelines, protocol requirements, regulatory standards, and sponsor procedures.

Key Responsibilities

Selected candidates will:

• Develop strong relationships with investigators and clinical trial sites
• Perform site monitoring and clinical site management activities
• Ensure compliance with ICH-GCP, sponsor SOPs, and local regulatory requirements
• Gain complete understanding of study protocols and clinical procedures
• Coordinate with cross-functional teams for site readiness activities
• Support site selection and site validation processes
• Conduct remote and on-site monitoring visits
• Ensure clinical trial data accuracy, completeness, and integrity
• Protect subject safety, rights, and well-being during clinical trials
• Conduct initiation visits, monitoring visits, close-out visits, and follow-up activities
• Maintain proper clinical documentation and monitoring reports
• Review and monitor regulatory documents throughout the study lifecycle
• Coordinate with investigators and site staff regarding protocol deviations and recruitment activities
• Handle compliance issues, quality concerns, and site performance escalations
• Support audit and inspection readiness activities
• Maintain study information in CTMS, eTMF, and clinical systems
• Collaborate with pharmacovigilance, regulatory affairs, legal, finance, and operations teams

Clinical Trial Monitoring Functions

The role includes:

• Clinical trial monitoring
• Site performance tracking
• Regulatory documentation management
• Clinical compliance monitoring
• Subject safety oversight
• Protocol adherence checks
• Clinical data review
• Inspection readiness support

Career Growth Opportunities

Professionals in this role can build careers in:

• Clinical Research Associate (CRA)
• Clinical Trial Management
• Clinical Operations
• Pharmacovigilance
• Regulatory Affairs
• Clinical Project Management
• Site Management
• Global Clinical Research

Eligibility / Qualifications

Educational Qualification

Candidates should possess a degree in Life Sciences or healthcare-related disciplines.

Eligible Qualifications

• B.Pharm
• M.Pharm
• Pharm D
• B.Sc Life Sciences
• M.Sc Life Sciences
• Biotechnology
• Biochemistry
• Microbiology
• Nursing
• Clinical Research
• Biomedical Sciences
• Allied Healthcare Sciences

Experience Requirement

Candidates with experience in:

• Clinical research
• Clinical trial monitoring
• Site management
• Clinical operations
• Pharmacovigilance
• Regulatory compliance

will be preferred.

Required Skills

Candidates should have knowledge of:

• ICH-GCP guidelines
• Clinical trial monitoring
• Clinical site management
• Protocol compliance
• Regulatory documentation
• Adverse event reporting
• Clinical data management
• CTMS and eTMF systems
• Clinical operations processes
• Communication and stakeholder management

Preferred Skills

• Clinical research methods
• Data reporting and analysis
• Protocol adherence management
• Regulatory compliance oversight
• Team collaboration and mentoring

Location & Salary

Job Location

• India

Work Mode

• Flexible clinical research work arrangement based on project requirements

Expected Salary

Based on current pharmaceutical and CRO industry standards in India, the estimated salary for Specialist Clinical Research Associate roles may range between:

• ₹8 LPA to ₹16 LPA

Salary may vary depending on:

• Clinical research experience
• Monitoring expertise
• Therapeutic area exposure
• Regulatory knowledge
• Site management capabilities

Employee Benefits

MSD offers:

• Global clinical research exposure
• Career growth opportunities
• International research environment
• Healthcare and employee benefits
• Learning and development programs
• Exposure to global regulatory systems

Application Process

Interested candidates can apply directly through the official MSD careers portal:

Apply Here: https://jobs.msd.com/gb/en/job/MSD1GBR398007ENGB/Specialist-Clinical-Research-Associate?utm_source=linkedin&utm_medium=phenom-feeds

Candidates are advised to:

• Update their latest resume before applying
• Highlight clinical trial monitoring experience clearly
• Mention therapeutic area expertise
• Include ICH-GCP and clinical compliance exposure
• Add CTMS/eTMF experience if applicable

Frequently Asked Questions (FAQs)

1. Which company is hiring for this CRA role?

MSD is hiring for the position of Specialist Clinical Research Associate.

2. What is the role offered?

The company is hiring for Specialist Clinical Research Associate positions.

3. Which qualifications are eligible?

Candidates from Pharmacy, Clinical Research, Biotechnology, Life Sciences, Nursing, and allied healthcare backgrounds can apply.

4. Is clinical research experience required?

Yes. Candidates with relevant clinical research and monitoring experience are preferred.

5. What are the major responsibilities in this role?

Responsibilities include site monitoring, clinical trial management, regulatory compliance, protocol adherence, and subject safety oversight.

6. What is the estimated salary for this role?

The estimated salary may range between ₹8 LPA to ₹16 LPA depending on candidate experience and clinical research expertise.

Summary

Company	MSD (Merck & Co.)
Department Vacancies	Specialist Clinical Research Associate
Qualification	B.Pharm, M.Pharm, Pharm D, Biotechnology, Nursing, Clinical Research, Life Sciences
Experience	Experienced Candidates Preferred
Location	India

Tagged as: Pharma Jobs in Mumbai