What are the responsibilities and job description for the Scientist, Study Co-ordination position at Worldwide Clinical Trials?
What the Scientist, Study Coordination
A Scientist, Study Coordination works under minimal supervision and assists Bioanalytical Study Management Team who oversee the conduct of regulated and non-regulated studies. They assist with study management as directed by the Head of Bioanalytical Study Management, and / or Bioanalytical Study Management Team and serve as a liaison between Bioanalytical Study Management, Study Coordination, Quality Control Reviewers, Quality Assurance Auditors, and Document Coordination staff to coordinate study assignments and ensure all applicable quality control timelines are met.
What you will do
- Ensure quality of deliverables including data, reports, and electronic files
- Draft written procedures and templates to maintain a standardized quality output.
- Assist in assigning studies, scheduling, and coordinating to maintain the flow of studies and to meet timelines.
- Assist with communications with analysts and other personnel involved in conducting the studies.
- Assist with cross-department communication as necessary to ensure adherence to current policies.
- Assist with the review of data using scientific judgment regarding the quality and integrity of data and records associated with assigned studies.
- Assist with conducting / ensuring the study is in accordance with applicable SOPs, GLPs, study plans, and protocols.
- Assist in writing, preparation, and review of Sample Analysis Plans, Validation Plans, Analytical Test Methods, reports, SOPs, and protocols.
What you will bring to the role
Your experience
