Onsite Clinical Research Associate II — Trials Expert

Corcept Therapeutics; Redwood City (CA); On-site; USD 129,400 - 152,300; Full time

Job summary

Corcept Therapeutics in Redwood City, California is hiring a Clinical Research Associate II to monitor clinical study activities and ensure compliance with Good Clinical Practices and study protocols. The selected candidate will supervise study preparation, coordinate clinical trial components, and liaise with vendors and team members.

Applicants should have a BS/BA in science or healthcare, along with 3+ years of CRA experience, preferably in big pharma. The role offers a salary range of $129,400 – $152,300, based on experience and skills.

Qualifications

• 3+ years’ experience as a CRA or field monitor, especially in big pharma or CRO.
• Additional experience in the pharmaceutical industry is desirable.

Responsibilities

• Supervises study preparation and site preparation.
• Ensures GCP compliance throughout the clinical program.
• Acts as liaison with clinical vendors and team members.
• Coordinates cross-functional components of the clinical trials process.
• Drafts informed consent forms and ensures protocol compliance.

Skills

Knowledge of the clinical trials process

Excellent verbal and written communication skills

Ability to handle multiple tasks

Knowledge of GCP regulatory requirements

Education

BS / BA in science or health care field or RN

Job description

Corcept Therapeutics in Redwood City, California is hiring a Clinical Research Associate II to monitor clinical study activities and ensure compliance with Good Clinical Practices and study protocols. The selected candidate will supervise study preparation, coordinate clinical trial components, and liaise with vendors and team members.

Applicants should have a BS/BA in science or healthcare, along with 3+ years of CRA experience, preferably in big pharma. The role offers a salary range of $129,400 – $152,300, based on experience and skills.