IQVIA is a multinational company that provides advanced analytics, technology solutions, and contract research services to the healthcare industry. With a presence in over 100 countries, IQVIA combines data science and human science to help clients in the pharmaceutical, biotechnology, and medical industries make informed decisions. The company is known for innovation in clinical trials and healthcare analytics, making it a top choice for career opportunities in clinical research.
Job Responsibilities
As a Clinical Process Coordinator, your primary responsibilities will include:
- Supporting clinical operations and trial management processes.
- Coordinating with clinical teams to ensure accurate data collection.
- Assisting in maintaining clinical documentation and reports.
- Ensuring compliance with industry standards and protocols.
- Managing timelines and coordinating across teams to ensure smooth project execution.
Qualification
To qualify for the position of Clinical Process Coordinator at IQVIA, candidates must meet the following criteria:
- A Life Sciences graduate with a relevant degree (B.Sc., B.Pharm, or similar).
- No prior experience is required as the role is open to freshers.
Skills Required
To succeed in this role, the following skills are highly recommended:
- Strong communication skills: You will be coordinating with various teams, so clear communication is essential.
- Organizational skills: Ability to manage tasks and timelines effectively.
- Attention to detail: Ensuring that all data is accurate and documentation is up-to-date.
- Basic knowledge of clinical research: Understanding of clinical trials and research processes will be a plus.
- Tech-savviness: Familiarity with data management software and tools.
How to Apply
Interested candidates who meet the qualification criteria can apply by sharing their updated resume to the following email:
- Email: sherry.thammappakm@iqvia.com
