IQVIA is hiring for an Associate Project Manager / Associate Laboratory Project Services Manager role supporting clinical trial laboratory projects in India. The opportunity is listed across Thane, Ahmedabad and Bengaluru, with the supplied job listing indicating 5–10 years of experience and 10 openings.
The role is particularly relevant for professionals with backgrounds in clinical research, clinical trials, laboratory operations, project management and life sciences. IQVIA’s currently indexed version of the position identifies it as Assoc Lab Project Svcs Mgr, with a hybrid work arrangement and responsibility for laboratory aspects of assigned clinical trial projects.
The position involves study start-up, project planning, customer communication, laboratory operations, study documentation, issue management, clinical-trial milestones and study closeout.
Important: The job advertisement supplied for this article states 5–10 years of experience, while the currently indexed IQVIA version specifies 2+ years of clinical/research industry experience, including project-management or project-setup experience. Candidates should verify the experience requirement in the application portal before applying.
IQVIA Associate Project Manager Job Details
| Details | Information |
|---|---|
| Company | IQVIA |
| Position | Associate Project Manager / Assoc Lab Project Svcs Mgr |
| Industry | Pharmaceutical & Life Sciences |
| Department | Research & Development |
| Employment | Full Time, Permanent |
| Work Model | Hybrid |
| Locations | Thane, Ahmedabad, Bengaluru |
| Experience | 5–10 years as per supplied listing |
| Education | B.Sc, B.Pharm, M.Sc, M.Pharm and related Life Sciences qualifications |
| Openings | 10 |
| Salary | Not disclosed |
| Estimated salary range | ₹8–15 LPA* |
*The ₹8–15 LPA figure is an editorial market estimate only and is not stated by IQVIA in the supplied vacancy.
What Does an Associate Project Manager at IQVIA Do?
The Associate Project Manager will manage laboratory-related activities associated with clinical trial projects and act as an important point of contact between IQVIA, customers and operational teams.
The position covers the entire study lifecycle, including study start-up, maintenance and closeout. The role also requires coordination of project timelines, risks, issues, documentation, budgets and deliverables.
IQVIA’s indexed vacancy describes the position as responsible for managing laboratory aspects of assigned clinical trial projects and maintaining customer relationships throughout the study lifecycle.
IQVIA Associate Project Manager Responsibilities
1. Study Setup and Planning
The selected candidate will:
- Support clinical study setup and planning.
- Review protocols and budgets.
- Lead project meetings.
- Develop project plans and milestone schedules.
- Maintain risk, issue and action logs.
- Coordinate with study setup teams.
- Oversee protocol-specific documentation.
- Prepare materials for Kick-Off and Investigator Meetings.
2. Clinical Trial Monitoring and Closeout
Responsibilities include:
- Monitoring project plans, timelines and deliverables.
- Managing study documentation throughout the project lifecycle.
- Supporting eTMF filing activities.
- Monitoring study reporting.
- Organizing meetings with customers and study teams.
- Managing scope changes.
- Monitoring budget and quality.
- Addressing service-related issues.
- Capturing and sharing lessons learned.
3. Customer and Stakeholder Management
The Associate Project Manager will also:
- Develop and maintain customer relationships.
- Serve as an escalation point for study-level issues.
- Coordinate and triage study-specific problems.
- Work with multiple internal operational teams.
- Support customer surveys and health checks.
- Maintain effective communication with study stakeholders.
4. Training and Meetings
The position may involve:
- Participating in Investigator Meetings.
- Representing IQVIA during internal and external meetings.
- Supporting audits and inspections.
- Providing study-related training to sites, CRAs and customers.
- Maintaining communication with clinical research sites.
- Supporting process-improvement initiatives.
- Training less-experienced team members.
IQVIA Associate Project Manager Eligibility
According to the supplied job description, candidates should preferably have a Bachelor’s degree in Life Sciences or a related discipline along with relevant clinical research, project management or laboratory experience.
The listing specifically identifies the following educational backgrounds under the education section:
- B.Sc
- B.Pharm
- M.Sc
- M.Pharm
- Other relevant Life Sciences or related qualifications
The indexed IQVIA version similarly specifies a Bachelor’s degree in Life Sciences or a related field, while allowing an equivalent combination of education, training and experience.
Experience Required
The supplied Naukri listing states 5–10 years, whereas the currently indexed IQVIA posting mentions 2+ years of clinical or research industry experience, including project management/project setup experience preferred.
Therefore, professionals should check the final application page for the applicable experience criterion.
Key Skills Required
Candidates should ideally possess:
- Clinical Research
- Clinical Trial Management
- Project Management
- Laboratory Operations
- Central Laboratory Operations
- Customer Management
- Stakeholder Management
- Risk Management
- Issue Management
- Study Start-Up
- Clinical Trial Documentation
- eTMF
- Medical Terminology
- Project Planning
- Budget Monitoring
- Microsoft Office
- Communication Skills
- Team Coordination
Knowledge of central laboratory activities such as kits and supplies, logistics, specimen storage, laboratory operations, data transfers and site alerts is particularly relevant to this position.
Who Can Apply for This IQVIA Job?
This opportunity can be considered by experienced professionals from areas such as:
B.Pharm professionals with clinical research, clinical operations, laboratory project coordination or related experience.
B.Sc/M.Sc Life Sciences professionals with clinical research, laboratory or project-management experience.
M.Pharm professionals with relevant clinical research, laboratory or project-management exposure.
Professionals working in CROs, clinical research organizations, central laboratories, pharmaceutical companies and healthcare research environments may find the role particularly relevant.
Experience managing or coordinating Phase I–IV clinical trials is preferred.
Salary for IQVIA Associate Project Manager
IQVIA has not disclosed the salary in the supplied job listing.
For informational purposes, PharmaBharat estimates a potential range of approximately ₹8–15 LPA, depending on location, relevant experience, clinical research expertise, project-management responsibilities and the candidate’s existing compensation.
This is not an official IQVIA salary figure. Candidates should rely on the offer communicated during the recruitment process.
Work Location and Work Model
The supplied listing mentions:
- Thane, Maharashtra
- Ahmedabad, Gujarat
- Bengaluru, Karnataka
The role is described as Hybrid.
The currently indexed IQVIA version specifically lists Bengaluru as a hybrid position and indicates an evening shift starting from 5 PM onward.
Why This Role Is Important for Clinical Research Professionals
The position offers exposure to several critical areas of clinical development, including clinical trial project management, central laboratory operations, customer management, study documentation, risk management and study lifecycle management.
IQVIA’s laboratory operations include capabilities such as hematology, coagulation, chemistry, urinalysis, toxicology, special chemistry and specimen management, demonstrating the broader laboratory infrastructure surrounding its clinical research operations.
For professionals looking to transition from operational clinical research roles into clinical project management, this type of position can provide valuable cross-functional exposure.