Minimum Qualifications
Education:
Bachelor’s degree in a life science field is required.
Years of Experience:Typically requires 5 years of experience in clinical research, including a minimum of 2 years field monitoring experience and 3 years in lead CRA role.
Required Skills & Abilities:
- Excellent knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, & company SOPs.
- Excellent knowledge of therapeutic area assigned.
- Excellent knowledge of ICH/GCP Guidelines & EDC process.
- Strong verbal & written communication skills.
- Ability to train others in using MS Office Suite & EDC systems.
- Ability to meet deadlines, multitasks & prioritize based on study needs.
- Ability to make sound decisions based on available information.
- Ability to establish rapport with site personnel/ colleagues.
- Ability to work both in a team & independently.
- Ability to facilitate team meetings & teleconferences.
- Ability to present at internal study team meeting(s).
- Ability to train & mentor junior CRAs.
- Ability to seek new learning opportunities within & outside of the assigned project.
- Ability & willingness to travel.
All your information will be kept confidential according to EEO guidelines.
