Clinical Research Associate (CRA)

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators.
In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing’s syndrome).
Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation.
What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease.
The Clinical Research Associate (CRA) monitors clinical study activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols. This is a hybrid role that typically requires on-site presence three days per week.
Responsibilities

Supervises study preparation, site preparation and the in clinic phases directly or through a CRO for assigned studies
Ensures that GCPs and Corcept clinical SOPs are met throughout the clinical program
Acts as liaison with clinical vendors and other functional area team members to meet project goals
Coordinates cross-functional components of the clinical trials process such as drug product supplies, etc.
Participates in the preparation and negotiation of clinical trial agreements and study budgets
Produces RFPs and participates in the evaluation and negotiation of bids from prospective vendors
Shares protocol writing with the medical director and biostatistician and ensures that all boilerplate requirements are met
Drafts informed consent forms ensuring that they are in agreement with the protocols
Participates in the development of study related documents including CRFs, study manuals and related documents
Coordinates all study start up activities, potentially with and through the CRO Participates in site management and monitors study sites in the field with the CRO or independently on an as needed basis
Collects, reviews and tracks essential trial documents
Provides the clinical team and the program team with information regarding CRO and clinical site performance and recommend remediation when needed
Participates in study management to ensure study project goals are met

Preferred Education & Experience

BS / BA (science or health care field) or RN
3+ years’ experience as a CRA or field monitor at least some of which was in a big pharma or big CRO setting
Additional experience in the pharmaceutical industry is desirable

Preferred Skills & Experience

Knowledge of the clinical trials process, the application of SOPs, and medical terminology Therapeutic and protocol knowledge
Excellent verbal and written communication skills
Knowledge of GCP regulatory requirements
Knowledge of drug product supply requirements
Ability to handle multiple tasks with competing priorities
Ability to utilize a wide range of computer applications and tools

The pay range that the Company reasonably expects to pay for this headquarters-based position is $102,700-$120,900; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Applicants must be currently authorized to work in the United States on a full-time basis.
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Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.
Please visit our website at: https://www.corcept.com/
Corcept is an Equal Opportunity Employer
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