About the role

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. 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.

Before you apply

Applying takes about a minute. These four things decide how fast it moves after that.

Your profile is current

It's what we read first. Occupations, seniority and locations matter more than a long history.

Two examples you can talk through

Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.

A number in mind

What you're on now and what would make you move. We negotiate better when we know both.

Your notice period

Employers plan around it, and it's the question that stalls offers most often.

Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.

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