Merck Recruitment 2026 brings an opportunity for qualified professionals to join the company as a Senior Analyst – Clinical Trial Coordinator in Bangalore, Karnataka. The position is part of Merck’s Local-Regional Studies Support Office and focuses on supporting the smooth coordination and administration of clinical trial activities.
The selected candidate will work with dedicated clinical trial teams across local and regional studies. The role involves supporting activities such as budget and invoice tracking, quality issue management, regulatory reporting oversight and other operational coordination tasks required for effective clinical trial execution.
This position can be suitable for candidates with an academic background in a scientific field and early professional experience in clinical research. The role also offers exposure to an international, multicultural working environment.
Merck Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Merck |
| Job Title | Senior Analyst – Clinical Trial Coordinator |
| Job ID | 303686 |
| Location | Bangalore, Karnataka, India |
| Work Mode | Hybrid |
| Employment Type | Full Time |
| Experience | 1–2 years in a clinical research-related role |
| Qualification | Bachelor’s degree or equivalent in a scientific field |
| Industry | Healthcare / Life Science |
| Department | Local-Regional Studies Support Office |
| Salary | Not Specified |
About Merck
Merck is a global science and technology company working across Healthcare, Life Science and Electronics. Its Healthcare business focuses on developing medicines, intelligent devices and innovative technologies designed to support patients across different stages of life.
The company operates internationally and works across therapeutic areas including Oncology, Neurology and Fertility. Merck emphasizes scientific innovation, collaboration, inclusion and opportunities for professional growth.
Job Description
The Senior Analyst – Clinical Trial Coordinator will support clinical trial teams with a variety of operational and administrative activities. The role is designed to help ensure that assigned studies remain organized, compliant and on schedule.
Working under the guidance of senior team members, the Clinical Trial Coordinator will contribute to activities related to financial tracking, quality support, regulatory reporting and general trial coordination.
The position requires strong attention to detail, effective communication and the ability to manage multiple activities within established timelines.
Senior Analyst – Clinical Trial Coordinator
As part of the Local-Regional Studies Support Office, the candidate will coordinate and support essential activities associated with local and regional clinical studies.
The role provides an opportunity to build practical knowledge of clinical development operations while contributing to the quality and integrity of clinical trial processes.
Eligibility Criteria
Candidates interested in this Merck opportunity should meet the following requirements:
- A Bachelor’s degree or equivalent qualification in a scientific field.
- Approximately 1–2 years of experience in a clinical research-related position.
- Candidates without a degree may also be considered with at least 3 years of relevant professional experience.
- Non-degree candidates should also have additional qualifications demonstrating exposure to clinical research fundamentals.
- Basic understanding of clinical operations.
- Familiarity with ICH-GCP guidelines.
- Ability to work effectively within a structured clinical trial environment.
Skills and Qualifications
Candidates should possess a combination of clinical research knowledge, organizational ability and communication skills.
Important skills include:
- Basic knowledge of clinical trial operations.
- Understanding of ICH-GCP principles.
- Familiarity with clinical trial administrative processes.
- Proficiency in standard office productivity tools, including spreadsheet, word-processing and presentation applications.
- Some familiarity with clinical trial management systems.
- Strong written and verbal communication skills in English.
- Ability to communicate effectively with teams across different functions and countries.
- Excellent organizational and time-management skills.
- Strong attention to detail.
- Ability to manage high-volume tasks while maintaining accuracy and quality.
- Ability to work independently as well as collaboratively.
- Comfort working in an international and multicultural matrix organization.
- Proactive approach to assigned responsibilities.
- Willingness to ask questions and seek clarification when required.
- Adaptability and willingness to continuously develop professional knowledge.
Key Responsibilities
The Senior Analyst – Clinical Trial Coordinator may be involved in the following activities:
- Supporting clinical trial teams across local and regional studies.
- Coordinating essential operational activities associated with assigned trials.
- Tracking clinical trial budgets and related financial information.
- Supporting invoice tracking and associated administrative processes.
- Assisting with the management and follow-up of quality-related issues.
- Supporting oversight of regulatory reporting activities.
- Maintaining accurate and organized trial-related information.
- Coordinating information between relevant internal stakeholders.
- Helping ensure assigned activities are completed within required timelines.
- Following applicable clinical research procedures and quality requirements.
- Supporting the operational integrity of clinical development activities.
- Working with senior colleagues to develop knowledge and expertise in clinical trial operations.
- Contributing to continuous improvement and effective execution of assigned responsibilities.
Work Location and Work Environment
The position is based in Bangalore, Karnataka, India.
- Work Mode: Hybrid
- Employment Type: Full Time
- The role involves collaboration with teams across different functions and geographical regions.
- The position operates within an international and multicultural work environment.
- Specific working hours or shift timings have not been mentioned in the available vacancy details.
Salary / CTC
The salary or CTC for the Senior Analyst – Clinical Trial Coordinator position has not been specified in the provided job information.
Candidates should check the official recruitment communication for details regarding compensation and other employment terms.
Selection Process
The detailed selection process has not been provided in the available vacancy information.
Candidates should follow the employer’s official recruitment process and be prepared to discuss their education, clinical research experience, knowledge of clinical operations, ICH-GCP understanding and relevant professional skills.
How to Apply
Interested and eligible candidates should apply through the official Merck recruitment process for Senior Analyst – Clinical Trial Coordinator, Job ID 303686.
Before submitting an application, candidates should:
- Review the eligibility requirements carefully.
- Ensure that their educational qualifications meet the stated criteria.
- Highlight relevant clinical research or clinical operations experience in their resume.
- Provide accurate educational and professional information.
- Complete the application through the official Merck careers channel.
Important Details Before Applying
- Company: Merck
- Position: Senior Analyst – Clinical Trial Coordinator
- Job ID: 303686
- Location: Bangalore, Karnataka, India
- Work Mode: Hybrid
- Employment Type: Full Time
- Degree Requirement: Bachelor’s degree or equivalent in a scientific field.
- Experience: 1–2 years of clinical research-related experience for degree holders.
- Alternative Eligibility: Candidates without a degree may be considered with at least 3 years of relevant professional experience and additional qualifications related to clinical research fundamentals.
- Clinical Knowledge: Understanding of clinical operations and ICH-GCP.
- Communication: Strong English communication skills.
- Salary: Not specified in the available job details.
Important Note
Recruitment requirements, vacancy status, application conditions and other employment details may be subject to change. Candidates are advised to verify the latest information through the official Merck recruitment source before applying.
FAQs – Merck Senior Analyst Clinical Trial Coordinator Recruitment 2026
1. What is the position available at Merck?
Merck is recruiting for the position of Senior Analyst – Clinical Trial Coordinator.
2. What is the Job ID for this vacancy?
The Job ID is 303686.
3. Where is the Senior Analyst Clinical Trial Coordinator position located?
The job is based in Bangalore, Karnataka, India.
4. Is this a full-time job?
Yes. The position is listed as Full Time.
5. Is the Merck Clinical Trial Coordinator position hybrid?
Yes. The vacancy specifies a Hybrid work arrangement.
6. What qualification is required for this position?
Candidates should have a Bachelor’s degree or equivalent in a scientific field. Candidates without a degree may also be considered with at least three years of relevant professional experience along with additional qualifications demonstrating exposure to clinical research fundamentals.
7. How much experience is required?
Candidates with the required degree should generally have 1–2 years of experience in a clinical research-related role. Candidates without a degree may be considered with a minimum of 3 years of relevant professional experience.
8. Is knowledge of ICH-GCP required?
Yes. Candidates should have a foundational understanding of clinical operations and ICH-GCP guidelines.
9. What skills are important for this role?
Strong organization, attention to detail, English communication, office software proficiency, basic clinical trial knowledge, teamwork and the ability to work effectively in an international environment are important for this position.
10. Has Merck mentioned the salary for this vacancy?
No specific salary or CTC has been provided in the available job details. Candidates should refer to the official recruitment communication for compensation information.