Senior Clinical Research Associate (Western Region)

Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world’s premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others.

Position Summary:

The Senior Clinical Research Associate (Sr. CRA) will participate in the preparation and execution of Phase 1-3 clinical trials. The Sr. CRA oversees the progress of clinical investigations by conducting site qualification, initiation, interim, and close-out visits. The Sr. CRA monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by Crinetics Pharmaceuticals and partner CRO(s). The Sr. CRA works closely with the Clinical Trial Manager (CTM) and Clinical Monitoring management to ensure all monitoring activities are conducted according to study requirements. The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits, internal CRA training and evaluation visits, and CRO monitoring visit report reviews.

Essential Job Functions and Responsibilities:

These may include but are not limited to:

• Develop strong, collaborative investigational site relationships and ensure continuity of relationships through all stages of the trial.

• Perform clinical study site management/monitoring activities efficiently in compliance with GCP/ICH requirements, SOPs, local laws and regulations, protocol, Clinical Monitoring Plan, and associated documents.

• Participate and provide input on site selection and site qualification activities.

• Coordinate and manage assigned tasks in collaboration with the study team to achieve site activation.

• Perform remote and on-site monitoring activities using various tools to ensure subject rights, safety, and well-being are protected as well as the reliability and integrity of study data.

• Conduct site visits including but not limited to qualification visits, initiation visits, interim monitoring visits, and close-out visits; generate clear, comprehensive, and accurate visit reports and letters in a timely manner.

• Review and verify study records including source documents, case report forms, informed consent forms, and other materials to ensure the data is complete and accurate.

• Interact with the clinical study sites to resolve data queries and/or data entry errors and obtain additional information on potential serious adverse events.

• Assess and monitor investigational product receipt, storage, administration, accountability, and return processes.

• Collect, review, and monitor essential regulatory documentation maintained by the site for study start-up, study maintenance, and study close-out.

• Submit site essential documents to the TMF following inline quality review and resolve any quality issues related to submitted documents.

• Train and assist site coordinators, investigators, and CRO (as applicable) in collecting data and executing the study in a timely manner that meets the protocol requirements and timelines/milestones; serve as a resource to site coordinators, investigators, and other staff members regarding investigational products and protocols.

• Communicate and document contacts with investigators and site staff regarding issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, adverse event reporting, site audits/inspections, and overall site performance.

• Identify, assess, and resolve site performance, quality, or compliance problems and escalate as needed per the defined escalation pathway in collaboration with CTM and/or Clinical Monitoring management.

• Assist in the development and implementation of subject enrollment and recruitment strategies for the site.

• Manage and maintain visit information such as site/subject visit tracking and other documentation in the Clinical Trial Management System (CTMS), Trial Master File (eTMF), and other systems.

• Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics, office and travel expense submissions, and approvals as needed).

• Ensure internal and study-related traini