Clinical research associate
Adex Personnel is seeking a Clinical Research Associate for a company working in the field of medical technology innovation.
The individual will play an important role in the conduct of clinical trials and data management while supporting the on-site clinical trial management processes. Possibility of telecommuting.
Responsibilities:
- Participate in the development of clinical investigation plans and clinical observation instructions and forms (CRF);
- Participate in the development and implementation of monitoring plans, and prepare a checklist of study requirements;
- Performs clinical investigation monitoring, site opening, routine monitoring in accordance with monitoring plan, GCP, SOPs and regulatory requirements;
- Review site records and observation forms to ensure compliance;
- Ensure transmission and integrity of clinical data to the data management center;
-Follow-up on site performance by ensuring the application of measurement standards and see to the writing of reports following a follow-up visit. Write a corrective action plan to avoid errors or discrepancies;
-Participate in clinical site closures and archiving of study documentation and correspondence.
Desired skills:
- University degree in pharmaceutical development or other related training;
- Thorough knowledge of clinical development processes;
-Excellent knowledge of practices and principles related to the conduct of clinical trials according to ICH/GCP or other regulations;
- Experience in clinical site monitoring (a strong asset);
- Advanced level of English;
- Willingness to travel on a regular basis (in the current environment, the position is telecommuting).
Benefits :
-Flexible schedule;
-Possibility of telecommuting;
-Full range of insurance coverage;
Innovative and team-oriented work environment;
-Opportunity to join a company involved in a very innovative environment!
Please note that only selected candidates will be contacted.