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.