The scope of responsibilities will include:
- Constantly maintain and generate relations with Investigative Sites;
- Maintain and refine the internal site database in cooperation with Study Startup Clinical Operations and Process Improvement;
- Participate in development of improvement strategies for the site identification process;
- Create the initial list of potential sites;
- Communicates with project teams to define strategy and methodology of initial and followup site contacts;
- In cooperation with the project team maintain a study site identification tracker;
- Liaise with project teams to evaluate status and progress of site identification to identify and highlight any potential risks or issues to timelines or objectives;
- Perform due diligence check of regulatory limitations applicable to the recommended investigators or clinical sites.
- Participate in project team meetings during study startup as needed;
- Support the project team throughout study startup and further on.
Qualifications :
- University/college degree (life sciences/healthcare field is a plus) or an equivalent combination of education training and experience that presents the required knowledge skills and abilities
- Experience in site identification site management CRA activities and/or study startup activities preferred
- Knowledge of Good Clinical Practice local laws and applicable regulations in the region is a plus;
- Full working proficiency in English
- Excellent written and oral communication skills as well as time management skills.
- Organizational and attention to detail skills required
- Strong interpersonal and communication skills
Additional Information :
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
Remote Work :
Yes
Employment Type :
Fulltime