
Clinical Research Specialist
1 day ago
As a clinical research specialist, you will be responsible for writing and editing high-quality documents related to clinical trials. You will work under guidance to produce reports, updates, and other documentation that meet internal company standards and external regulatory guidelines.
Key Responsibilities:
- Write and edit clinical study reports, development safety update reports, and clinical trial registration documents.
- Act as a documentation consultant in clinical trials to ensure compliance with company standards and regulatory guidelines.
- May act as a liaison between clinical trials teams and publishing teams to ensure timely delivery of final documents.
- Report technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt.
- Distribute marketing samples where applicable.
- Prepare publications to satisfy regulatory requirements for publication of clinical trial results.
Requirements:
- Minimum life-science degree or equivalent (BSc) with 4 years of clinical research experience.
- MSc/MPharm with 2 years of clinical research experience.
- Desirable qualifications include a doctoral degree, qualification in medical sciences, or MBBS/MD equivalent.
Benefits:
We offer a range of benefits to support your career and well-being, including opportunities for professional growth and development, competitive compensation and benefits packages, and a collaborative work environment.
How to Apply:
If you are interested in this role, please submit your application through our website.
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