CLINICAL RESEARCH ASSOCIATE

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. 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.

Additional Information: All your information will be kept confidential according to EEO guidelines.