Ref. #HCT-CRA-2101
Required:
- University degree in Health Sciences
- AT least 6 months of experience as Clinical Research Associate
- High level of English, written and spoken
- Microsoft Office regular user
- Availability to travel
Desirable:
- Complementary training in Clinical Research
Job Description:
As a CRA you will be responsible for the following activities:
- Management of study documents: presentation, follow-up and review
- Collaboration with site staff to ensure that clinical trials are being conducted in accordance with protocol, ICH, GCP and other applicable regulations
- Organization, participation and follow-up of meetings
- Initiation, monitoring and study closure activities at a local level
- Administrative support to other team members
Ref. #HCT-MW-1902
Required:
- University Degree in health sciences with PhD
- High level of English, both written and spoken
Desirable:
- Knowledge of statistics
- Previous experience as a medical writer in a pharmaceutical company or CRO
- Author of scientific publications
Job Description:
- Drafting of complex scientific documents, such as original or revision articles, summaries to congresses
- Layout of figures and tables
- Adapting manuscripts to the standards of each journal
- Creation of bibliographic databases
- Attendance at meetings with the client and project collaborators
- Continued support to authors during the publication process