Sr. Clinical Research Associate
- Job ID:
- Date:07/03/2008
- Location:
- State:Connecticut
- Degree:B.S./B.A.
- Current Professional Level:Sr. Manager/Manager
- Salary Range:$100,000 to $124,999
- This salary range was selected from the CareersInPharmaceutical.com salary data list. See the "Additional Salary" or contact the Recruiter for actual salary and benefits.
- Job Types:
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Clinical Research Associate
Job Description
Assists in the operational activities involved in the planning, conduct and completion of clinical trials. Uses some independent action and judgment to complete these activities. Such activities include: Establishing and ordering clinical supplies Establishing target dates for completion of assignments. Collection, review and filing of clinical trial documentation Preparation of all critical trial documents (e.g. monitoring guidelines, investigator site file and draft informed consent). Tracking and requesting grant payments Communication with investigative sites on routine matters concerning on-going trials. Handling requests for trial related information. Adheres to governmental regulations and company SOPs when executing assignments. Working closely with data management, the clinical monitor and/or medical supervisor, the Clinical Research Associate performs the in-house review of clinical trial data to ensure the completeness, accuracy and consistency of the trial data. Ensures that all data discrepancies are resolved. Seeks input on issues requiring medical judgment. Responsible for in-house management of investigative sites. Assists the clinical monitor and/or medical supervisor in preparing clinical trial protocols, writing non-driven data sections of clinical trial reports and in the review and reconciliation of serious adverse event narratives. Develops, implements and continually reviews tracking systems for assigned projects to assure that timelines are being met as anticipated. Develops and maintains an active liaison with members of other groups involved in the drug development process, particularly data management and clinical field operations, and participates in Clinical Trial Team meetings. The incumbent is responsible for adhering to governmental regulations and guidelines and company SOPs in the conduct of clinical trials.
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