Hybrid Clinical Research Job at IQVIA
If you are searching for a Hybrid Clinical Research Job with a globally recognised organisation, this IQVIA career opportunity could be the right fit. IQVIA is hiring for the position of Clin Process Assoc/ Sr Clin Process Assoc in Kolkata, India. This full-time hybrid role is ideal for life sciences graduates with relevant experience who are looking to grow in clinical operations and project support within a structured and compliance-driven environment.
About Company
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. The company supports healthcare and pharmaceutical organisations in accelerating innovation and improving patient outcomes. With a strong global presence and deep expertise in clinical development, IQVIA offers professionals a dynamic environment to build a long-term clinical research career while contributing to high-impact clinical projects across therapeutic areas.
Job Details
| Particulars | Details |
|---|---|
| Company | IQVIA |
| Job Title | Clin Process Assoc / Sr Clin Process Assoc |
| Department | Clinical Process |
| Location | Kolkata, India |
| Employment Type | Full-Time |
| Work Mode | Hybrid |
| Qualification | Bachelor’s Degree in Life Sciences or a related field |
| Experience | Minimum 3 years of relevant experience |
| Reference Number | R1557192 |
Job Overview
Provide project-related assistance for assigned complex project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.
Job Description
This Clinical Research Job involves supporting complex clinical projects and ensuring smooth coordination between project teams and sites. The role focuses on maintaining documentation, tracking project timelines, and ensuring compliance with SOPs, policies, good clinical practices, and regulatory requirements.
The Clinical Process Associate will work closely with study teams to create and review study documents, manage internal systems and tracking tools, and contribute to high-quality deliverables within defined service level agreements (SLAs). The position also involves participating in team meetings, implementing action items, and maintaining effective project and site communication. This opportunity is well-suited for professionals who want hands-on exposure to clinical project operations in a structured global environment.
Key Responsibilities
- Perform complex processes and tasks that eventually result in high-quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
- Establish and maintain effective project/ site communications
- Create and maintain relevant project documents
- Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project-specific information
- Participate in document management (creation, review, maintenance, storage, as applicable)
- Coordinate and collaborate with various project stakeholders
- Review, evaluate and recommend modifications to designated processes
- Participate in (study) team meetings and implement action items
- Collaborate with the project lead/team members in creation/review of study documents
- Setting quality standards and reviewing deliverables to the same standards for process tasks
- Act as SME/mentor/buddy for new joiners and support with system/process trainings
- May be assigned the role of systems expert – guiding teams on the use of systems, creating guidance documents, updating relevant training, and any new updates available in the systems
- Relaying the training to the team and being available to address the queries for the teams
Eligibility Criteria
- Education: Bachelor’s Degree in life sciences or a related field
- Experience: Typically requires a minimum of 3 years of relevant experience.
- Additional Requirement: Requires knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education. 3 years of overall experience. Equivalent combination of education, training and experience.
Required Skills
- Knowledge of Good Clinical Practices (GCP)
- Understanding of regulatory requirements
- Documentation and project coordination skills
- Ability to manage timelines and tracking tools
- Process review and improvement capability
- Training and mentoring skills
- Strong communication and collaboration skills
- System handling and database management
How to Apply?
- Visit the official application link below
- Review the job details carefully
- Submit your online application through the portal
Why Join IQVIA?
A Clinical Research Job at IQVIA offers exposure to global clinical projects, structured processes, and a strong compliance-driven work culture. As a Clinical Process Associate, you gain experience in clinical documentation, project coordination, system management, and quality standards. The hybrid work model in Kolkata provides flexibility while allowing collaboration with experienced professionals. IQVIA’s global network and focus on innovation make it an excellent platform for long-term career growth in clinical research and operations.
Conclusion
If you are looking to advance your career through a Clinical Research Job with a reputed global organization, this IQVIA opportunity for Clin Process Assoc/ Sr Clin Process Assoc could be your next step. Explore this hybrid role in Kolkata and apply today to strengthen your clinical operations expertise.
