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Abbott Laboratories

# Senior Clinical Trial Manager

India > Mumbai: Mumbai Development Center - EPD Full-time Manager or lead Healthcare & Clinical 

Listed on Abbott Laboratories’s official careers site. Posted October 19, 2026. Check that it is still open and apply there.
[Apply on Abbott Laboratories’s careers site →](https://abbott.wd5.myworkdayjobs.com/abbottcareers/job/India--Mumbai--Mumbai-Development-Center---EPD/Senior-Clinical-Trial-Manager_31162716-1)

[OpenNash Jobs](https://jobs.opennash.com/) / [Abbott Laboratories](https://jobs.opennash.com/companies/abbott-laboratories/) / Senior Clinical Trial Manager

## Job description

### JOB DESCRIPTION
- Plan, coordinate and oversee all start-up activities of internal disciplines (Drug supply, Regulatory, Safety, Data Management etc.) and being the main contact (supervise, steer etc.) for involved CROs and other external vendors, if applicable Agree and/or ensure implementation of study principles and deliverables (safety, timelines, quality, milestones, budget, etc.) and follow-up to guarantee adherence
- Facilitate communication and ensure adequate collaboration between all involved parties
- Communicate effectively processes to in-/external service groups and clients in accordance with all applicable procedures (e.g.

BIOM, Task List etc.) Participate in teams related to trial conduct (e.g. Clinical Study team, Extended Joint Abbott- CRO Clinical Team, Drug supply team etc.) and organize/attend external key study meetings (Kick-off meeting, CRA meeting, Investigator meeting, etc) as applicable Read, review and/or assist in preparation of core project documents (e.g. Investigator Brochure, Concise Clinical Development Plan, Protocol, Informed Consent Form) as applicable Review key Clinical Trial Management strategies like: Communication plan / Feasibility / Patient & Site recruitment / Drug supply / EC&RA Submission, etc.
- Oversee and manage with the CRO Project Manager the study conduct in order to ensure adequate and timely delivery of study data and documentation in Trial Master File (TMF): Use efficiently tools to monitor status of e.g. patient recruitment and take corrective action if necessary
- Ensure respect of agreed deliverables, and communicate efficiently within the teams (timelines, milestones, budget, quality) Co-coordinate timely availability of all supplies important for the conduction of trials, including the re-supply of sites
- Monitor data collection, cleaning and data transfer with respect to completeness, quality and timely delivery of the final results
- Review audit reports and ensure issues are resolved
- Participate in strategic decision making to improve recruitment
- Apply operational risk management plan (if applicable)
- Support activities to generate study report / dossier
- Supervise and monitor the transfer and archiving of the clinical file (e.g.

TMF) The base pay for this position is N/A In specific locations, the pay range may vary from the range posted.

### JOB FAMILY

Clinical Affairs / Statistics DIVISION: EPD Established Pharma LOCATION: India > Mumbai: Mumbai Development Center - EPD ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

## At a glance
- Posted by the employer: Oct 19, 2026
- First seen by OpenNash: Oct 20, 2026
- Last checked: Oct 20, 2026
- Listed for: 1 day
- Location: India > Mumbai: Mumbai Development Center - EPD
- Employment type: Full-time[Apply on Abbott Laboratories’s careers site →](https://abbott.wd5.myworkdayjobs.com/abbottcareers/job/India--Mumbai--Mumbai-Development-Center---EPD/Senior-Clinical-Trial-Manager_31162716-1)

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