Medpace Recruitment 2026: Associate Clinical Trial Manager Jobs for PhD Graduates
Medpace Clinical Research India is seeking Associate Clinical Trial Managers (aCTM) to join their Navi Mumbai office. The post is aimed at Phds and those with post-doctoral experience in Cardiovascular, Renal, Metabolic or GI research. If you’re a recent PhD looking to move from academia into clinical trial management then this is the role for you.
Selected candidates will be assisting the Project Coordinators and Clinical Trial Managers with the various aspects of global clinical studies including project administration, study documentation, timelines and co-ordinating with sponsors, study sites and vendors.
Job Details
| Particulars | Details |
| Company | Medpace Clinical Research India |
| Job Role | Associate Clinical Trial Manager |
| Department | Clinical Trial Management |
| Qualification | PhD in Life Sciences |
| Experience | 0–3 years |
| Location | Navi Mumbai, Maharashtra |
| Employment Type | Full Time, Permanent |
| Work Environment | Office-based |
| Industry | Pharmaceutical & Life Sciences |
About Medpace
Medpace is a full service CRO providing Phase I to IV clinical development services to biotech, pharma and medical device companies.
Headquartered in Cincinnati, OH, Medpace operates in over 40 countries and provides clinical research support across a range of therapeutic areas including oncology, cardiology, metabolic, endocrine, CNS and infectious diseases.
Job Role and Responsibilities
As an Associate Clinical Trial Manager you’ll be supporting the Project Coordinators and Clinical Trial Managers in the management of clinical research projects. You’ll be responsible for the coordination of global study activities, ensuring that the project documentation is always up to date and that all tasks are completed on time.
Key responsibilities include:
- Communicate and work alongside Project Coordinators and Clinical Trial Managers on the global clinical study activities.
- Complete all the recurring project work accurately and on time.
- Compile and maintain project specific status reports in the CTMS.
- Co-ordinate with internal project teams, sponsors, clinical study sites and third party vendors.
- Provide oversight and quality control of the internal regulatory filing system.
- Support the management and oversight of clinical study supplies.
- Create and maintain project schedules.
- Arrange the project meetings and take the time to produce accurate meeting minutes.
- Support the administration and management of clinical trial projects.
Eligibility Criteria
Educational Qualification
- PhD in Life Sciences.
Research Experience
Candidates should have research experience in one or more of the following therapeutic areas:
- Cardiovascular
- Renal
- Metabolic
- Gastrointestinal
Recent Phds and postdocs with research experience are all very much encouraged to apply.
Experience Requirements
- The listing states an experience level of 0 to 3 years.
- You don’t need any prior experience in CRO or pharma, that will be an advantage though.
- Academic research experience in the relevant therapeutic areas is of course important.
Required Skills
- Fluency in English.
- Strong presentation and communication skills.
- Good organisational and administrative skills.
- Knowledge of Microsoft Word, Excel, Windows and databases.
- Ability to juggle multiple tasks and meet deadlines.
- Ability to work effectively in a fast paced environment.
- Ability to work with international teams.
- Strong analytical and problem solving skills.
Career Growth and Training
Medpace give recent Phds a chance to get into the clinical research industry and start a career in clinical trial management.
The position includes:
- Foundational training in clinical project administration and management.
- Intensive onboarding and training programmes.
- Office based learning with on-site mentors.
- Clear career paths and opportunities for progression.
- Continuous professional development and learning.
- Opportunities to work with international clinical research teams.
The role is for candidates who demonstrate they have the skills and the interest to progress into Clinical Trial Manager (ctm) responsibilities. This role is for candidates who show they have the skills and interest to grow into CTM responsibilities.
- Competitive compensation programs.
- Health and wellness benefits.
- Retirement benefits.
- Paid time off (PTO).
- Company-sponsored social events.
- Occasional work from home flexibility for eligible posts following training.
Benefits will vary from country to country.
Job Location
Office Address:
Floor 12, Gen 4/1, Unit No. 1203, Aurum Q Parc, Building Q2, Thane Belapur Road, TTC Industrial Area, Navi Mumbai, Maharashtra, India.
This is predominantly an office role, although eligible staff will be able to work from home at times after training.
How to Apply for Medpace Recruitment 2026
If you’re interested and meet the criteria you can apply via the Medpace recruitment listing.
- Open the job application link.
- Just go through the eligibility criteria and the job description.
- Complete the online application form.
- Upload your updated CV and academic details.
- Submit the application for consideration.
Medpace will be reviewing all applications and will be contacting those candidates whose profiles are a match for an interview.
Job Summary
| Category | Details |
| Company | Medpace Clinical Research India |
| Position | Associate Clinical Trial Manager |
| Qualification | PhD in Life Sciences |
| Experience | 0–3 years |
| Therapeutic Areas | Cardiovascular, Renal, Metabolic and Gastrointestinal |
| Location | Navi Mumbai, Maharashtra |
| Employment Type | Full Time, Permanent |
| Apply Mode | Online |
Frequently Asked Questions (FAQs)
1. What role is Medpace hiring for?
Medpace Clinical Research India are hiring for the Associate Clinical Trial Manager (aCTM) role.
2. What is the required qualification?
Candidates must have a PhD in Life Sciences.
3. What research backgrounds are preferred?
Must have research experience in Cardiovascular, Renal, Metabolic or Gastrointestinal therapeutic areas.
4. Can recent PhD graduates apply?
Yes, the role is specifically aimed at recent PhD grads looking to kick off a career in clinical trial management.
5. Is prior CRO experience a must?
No. Previous CRO or pharma industry experience is not a must have but would be an advantage.
6. Where is the job based?
The position is based at Medpace’s office in Navi Mumbai, Maharashtra.
7. What is the job experience range?
The job listing indicates an experience range of 0–3 years.
8. How can candidates apply?
Eligible candidates can submit their applications through the Medpace job listing on Naukri using the application link provided above.