IQVIA Hiring For Associate Project Manager

Pharmabharat; Thane; Hybrid; INR 800,000 - 1,500,000; Full time

Job summary

IQVIA in India is hiring for an Associate Project Manager / Associate Laboratory Project Services Manager to support clinical trial laboratory projects. The role spans Thane, Ahmedabad and Bengaluru with a hybrid work model and oversight of lab activities across the study lifecycle.

Ideal candidates hold a B.Sc, B.Pharm, M.Sc, M.Pharm or related Life Sciences degree and have 5–10 years of clinical research or project management experience.

Qualifications

• 5–10 years of experience in clinical research, laboratory projects or related fields.
• Bachelor’s degree in Life Sciences or a related discipline.
• Experience across the full study lifecycle in clinical trials.
• Hybrid work model and collaboration with cross-functional teams.

Responsibilities

• Oversee study setup and planning, including protocol review and milestone development.
• Monitor clinical trial progress, documentation, budgets and deliverables.
• Manage customer relationships and coordinate with internal teams across sites.
• Assist in investigator meetings, audits and training of staff.

Skills

Clinical research

Project management

Laboratory operations

Life sciences

Education

B.Sc

B.Pharm

M.Sc

M.Pharm

Life Sciences

Tools

Project Management Software

Job description

B.Sc, B.Pharm, M.Sc, M.Pharm and related Life Sciences

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.

Project Management

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Pharmaceutical

projects

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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.

Management

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.

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

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.

Jobs

What Does an Associate Project Manager at IQVIA Do?

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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.

Recruitment & Staffing

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.

1. Study Setup and Planning

The selected candidate will:

• Support clinical study setup and planning.
• Review protocols and budgets.
• 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:

Project Management Software

• 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:

Project Management

• 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.

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.

Management

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.

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.

Jobs

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.

Project Management Software

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:

Project Management

• Thane, Maharashtra
• Ahmedabad, Gujarat

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.

Management

For professionals looking to transition from operational clinical research roles into clinical project management, this type of position can provide valuable cross-functional exposure.