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4 days ago
We are seeking a detail-oriented Clinical Data Specialist to join our team. As a key member of our clinical data management group, you will be responsible for ensuring the quality and integrity of our clinical trial data.
The ideal candidate will have a strong background in clinical data management, with experience working on pharmaceutical or CRO trials. You will be responsible for leading clinical data management activities, collaborating with cross-functional teams, and ensuring timely and compliant data management processes.
Key Responsibilities:
- Liaise with study teams and vendors to ensure accurate and complete data collection.
- Develop and implement data cleaning and integrity monitoring plans.
- Analyze and resolve data discrepancies and queries.
- Maintain accurate and up-to-date documentation in the Trial Master File (TMF).
Qualifications:
- Bachelor's or Master's degree in Life Sciences, Pharmacy, Clinical Research, or related field.
- 3+ years of experience in Clinical Data Management within the pharmaceutical or CRO industry.
- Strong knowledge of EDC systems, clinical trial processes, and regulatory compliance (ICH-GCP).
- Excellent analytical, communication, and problem-solving skills.
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and detail-oriented individual with a passion for clinical data management, we encourage you to apply for this exciting opportunity.
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