Clinical Research Associate
The CRA is the go-between the investigator & the pharmaceutical company; ensuring that the study is conducted according the guidelines. He/she is monitoring the collected data in the patients’ files and the medical records, informing the investigator of incorrect or missing data. This job is requiring accuracy, good communication skills and flexibility.

Clinical Trial Assistant
The CTA is member of the project team and supports the Project Manager and CRA in-house. The CTA is responsible for the administrative part of the studies: correspondence, set-up documents, filing and archiving and additional tasks within the clinical project.

Project Manager
The PM is responsible for the coordination of all study related activities: budget monitoring, follow-up of the studies, pharmacovigilance and data processes.

Data Manager
The data manager handles the collected data, centralizes, verifies and validates the information in the clinical database for statistical processing. This job requires precision and patience. 

Pharmacovigilance Officer
The Pharmacovigilance Officer will ensure effective and accurate collection, database entry and reporting of safety data. The PO is responsible for the pharmacovigilance activities for assigned developmental and marketed products. 

Medical Advisor
The Medical Advisor provides a bridge between clinical research and the marketing and sales department as well as the remaining departments within the organization. He or she specifically provides an authoritative opinion and answers medically based questions concerning medical, legal and regulatory matters enabling colleagues to comply with the relevant statutory requirements.

Medical Science Liaison
A medical science liaison MSL is a person who acts as a bridge of communication between clinical medicine, and other areas of the healthcare industry, such as pharmaceutical or medical device company. The medical science liaison acts as an educator, combining clinical and commercial skills. 

Regulatory Affairs
Regulatory affairs officers combine knowledge of scientific, legal and business issues to ensure products, which are developed, manufactured or distributed by a wide range of companies, meet the required legislation. They advise on and coordinate the approval and registration of pharmaceuticals. They are the crucial link between their company, its products and regulatory authorities.