IQVIA is inviting applications for the position of Senior Lab Setup Coordinator. This exciting remote opportunity is ideal for professionals with experience in laboratory project setup, protocol interpretation, clinical trial operations, and laboratory database management.
Candidates with qualifications such as B.Pharm, M.Pharm, B.Sc, M.Sc, or Diploma and relevant laboratory setup experience can apply. The role offers exposure to advanced clinical trial technologies, AI-driven workflows, and global project management in the pharmaceutical and life sciences industry.
Job Highlights
- Position: Senior Lab Setup Coordinator
- Company: IQVIA
- Location: Remote (India)
- Experience Required: 4–7 Years
- Employment Type: Full-Time, Permanent
- Open Positions: 4
- Shift Timing: 5:00 PM onwards
- Industry: Pharmaceutical & Life Sciences
- Department: Healthcare & Life Sciences
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. With operations in over 100 countries and more than 86,000 employees worldwide, IQVIA helps healthcare organizations accelerate innovation and improve patient outcomes through data science and technology.
The company has been recognized among FORTUNE World’s Most Admired Companies and offers exceptional career growth opportunities for professionals in clinical research and laboratory operations.
Key Responsibilities
As a Senior Lab Setup Coordinator, you will:
- Lead laboratory database design, configuration, and validation activities.
- Manage laboratory project setup activities using Clinical Trial Management Systems (CTMS).
- Implement AI-enabled tools and automation to improve study setup efficiency.
- Collaborate with technology and innovation teams to deploy digital solutions.
- Support protocol amendments and sponsor-driven study changes.
- Ensure quality, accuracy, and timely delivery of laboratory setup deliverables.
- Conduct risk assessments and mitigation planning for project changes.
- Participate in process improvement and innovation initiatives.
- Coordinate with Data Management, Logistics, Clinical Operations, Laboratory Testing, and Technology teams.
- Provide technical guidance to sponsors and CRO partners.
- Translate complex technical concepts into actionable project solutions.
Required Qualifications
Educational Qualification
Candidates should possess any of the following:
- B.Sc (Any Specialization)
- Diploma (Any Specialization)
- B.Pharm
- M.Pharm
- M.Sc (Science)
Experience
- 4 to 7 years of relevant experience
- Strong laboratory setup experience
- Experience reading and interpreting clinical study protocols
- Knowledge of clinical trial systems and laboratory workflows
Preferred Skills
- Protocol Reading
- Lab Setup Experience
- Clinical Trial Management Systems (CTMS)
- Laboratory Database Configuration
- Clinical Research Operations
- Data Analytics
- AI and Automation Tools
- Project Coordination
- CRO and Sponsor Communication
- Risk Assessment and Change Management
Benefits of Working at IQVIA
- Work-from-home flexibility across India
- Exposure to global clinical trials and laboratory projects
- Career growth within a leading CRO and healthcare technology company
- Opportunity to work with AI-driven clinical research technologies
- Collaborative international work environment
- Professional development and training programs
How to Apply
Interested and eligible candidates can apply directly through the IQVIA careers portal or the job application link available on the official recruitment platform.
Hiring Office
IQVIA India
Omega Embassy TechSquare
Marathahalli-Sarjapur Outer Ring Road
Kadubeesanahalli
Bengaluru, Karnataka, India