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Clinical Research Associate Role
1 week ago
Key Responsibilities:
1. Oversee and monitor clinical trials, setting up, coordinating, and supervising studies.
2. Ensure that all aspects of the study are conducted according to the protocol, GCP (Good Clinical Practice), guidelines, and regulatory requirements.
How You Will Make an Impact:
1. Ensure validity of study by identifying/resolving discrepancies and obtaining missing data; may track core lab activities and more complex components of the trial.
2. Contribute to developing and writing clinical protocols, case report forms, and other study aids for investigational products by addressing issues by interacting with appropriate personnel.
3. Maintain expertise in regulations for applicable geographies and types of studies (IDE, non-significant risk, feasibility, exempt, etc.). Serve as a resource related to clinical trial regulations.
4. Ensure timely collection of study documentation by obtaining, maintaining, and controlling all necessary records and documentation according to procedures and regulations.
5. May mentor and train new employees as needed.
Requirements:
1. 4-year Undergraduate Degree or equivalent experience in Life Sciences, Biochemistry/Chemistry, Nursing, etc.
2. 3 – 6 years of related work experience is required.
3. Experience running cartridges and dealing with blood is preferred.
4. Science/Chemistry/Biochemistry and/or phlebotomy experience would be considered an asset.
5. Comfortable with frequent travel to study sites for clinical site visits.
Bonus Considerations:
1. A mechanical aptitude, good organizational skills, and an interest in continued learning is an asset.
2. Must be a self-starter and have the ability to follow instructions and use good judgment.
Total Compensation Package:
Weekly base pay + 4% vacation paid out weekly. Opportunity for travel and the chance to work with a reputable company in a fulfilling career.