Senior Clinical Data Safety Scientist
This is a role with a well-know Biopharmaceutical company in New Jersey. As a Senior Clinical Data Safety Scientist, you will perform quantitative and qualitative analysis of clinical data in support of study directors and their teams to develop innovative therapeutic products for the client.
Responsibilities in this role include:
- Ensure reported terms are recorded adequately
- Assigning of MedDRA and WHODD terms
- Post relevant queries for information
- Resolution of PT in SAE reconciliation in agreement with PDM and PV
- Perform coding and review coding listings in preparation for review and approval of study director
- Ensure all information is correctly captured in clinical database
Qualifications for this role include:
- Minimum of 8 years coding experience within clinical research
- Knowledge of coding systems such as INFORM, J-review; other clinical trial systems
- Proficiency with GCPs, other related regulations
- Strong understanding with ICH guidelines
- Proficiency with Good Clinical DM Practice
- Expertise with Microsoft Suite
If you are a senior coder within the clinical research industry, please do not hesitate to apply!
