Are you an experienced professional in clinical trials looking for an exciting opportunity? IQVIA, a global leader in healthcare technology and research, is currently hiring for the position of Senior Clinical Process Associate (Clinical Trial Assistant/Clinical Trial Associate). This is an excellent opportunity to join a dynamic team and contribute to impactful projects in the pharmaceutical and healthcare industries.
Position Details
- Job Title: Senior Clinical Process Associate (Clinical Trial Assistant/Clinical Trial Associate)
- Location: Bangalore/Thane, India
- Work Mode: Hybrid
- Experience Required: 2-3 years as a Clinical Trial Assistant
Key Responsibilities
As a Senior Clinical Process Associate, you will play a crucial role in supporting clinical trial operations. Your responsibilities include but are not limited to:
- Assisting in the planning, coordination, and execution of clinical trials.
- Ensuring accurate documentation and maintenance of trial master files.
- Communicating effectively with internal and external stakeholders to ensure smooth trial progress.
- Supporting regulatory submissions and compliance with GCP (Good Clinical Practice) guidelines.
- Managing timelines and providing updates on project milestones.
- Ensuring data quality and resolving discrepancies promptly.
Why Join IQVIA?
IQVIA is a recognized leader in healthcare research and technology solutions. Here’s why this opportunity is a perfect fit for ambitious professionals:
- Work in a hybrid environment offering flexibility and work-life balance.
- Collaborate with a talented and diverse team of professionals.
- Engage in meaningful projects that make a real difference in healthcare.
- Opportunity to grow and develop your career in clinical research.
Eligibility Criteria
To be considered for this role, candidates must meet the following criteria:
- Minimum of 2-3 years of experience as a Clinical Trial Assistant.
- Strong knowledge of clinical trial processes and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to multitask and work effectively under tight deadlines.
- Proficiency in relevant software and tools used in clinical trial management.
How to Apply
If you meet the qualifications and are passionate about advancing your career in clinical research, don’t miss this opportunity. Interested candidates are encouraged to share their updated resumes at navitha.gouli@iqvia.com.
