Senior Clinical Scientist

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. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. 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 Scientist will be working within a multi-disciplinary team focusing on a Clinical Development Program. This individual will provide clinical expertise and scientific insights to help monitor, track, and analyze subjects’ data in phase 1 - 3 studies. The incumbent will work closely with the Medical Lead and will collaborate with all the groups involved in Clinical Development e.g., Pharmacokinetics (DMPK), Clinical operations, Biometrics, Pharmacovigilance, and Medical Affairs. Essential Job Functions and

Responsibilities: These may include but are not limited to: Responsible for monitoring, tracking, and analyzing clinical trials subjects’ data, under the supervision of the Clinical Medical Lead. This involves collaborating with investigators, CRO medical monitors, Clinical Operations and the Biometrics team. Monitor, analyze, and review on a regular basis safety and efficacy data for events of interest or needing further investigation. Review laboratory and other safety parameters, review patient profiles, data listings, summary tables, and review coded terms. Collaborate closely with clinical leads and medical directors to align on scientific content and program strategy. Support authoring and review of protocols/amendments, protocol clarification letters, clinical study reports, IBs, ICFs, training documents, charters, lab and pharmacy manuals, newsletters, medical monitoring plans, statistical analysis plans, data management plans, eCRFs, eCRF completion guidelines, and other clinical and regulatory documents. Address questions regarding scientific and protocol related issues from investigators in consultation with Medical Monitors or the Medical Lead. Contribute to the preparation and/or review of safety narratives, manuscripts, and scientific presentations. Contribute to the preparation and/or review of regulatory submissions, responses, and requests for information. Support preparation for safety review committees, DSMBs/DMC including data review and development of presentations. In collaboration with Clinical Operations and the Medical Lead, review protocol deviations to identify cause and appropriate resolution. Participates in Database lock activities as assigned by MM (including data review and cross-checks to ensure quality and consistency) and represents CR at internal data management meetings. Contribute to the development of relevant sections of regulatory documents such as amendments to protocols, briefing books, safety updates, responses to Health Authorities questions. Collaborate with Medical Affairs and Patient Advocacy to support effective working relationships with key investigators, key opinion leaders and patient advocates. Participate in research site identification and relationship building with CROs in this space. Other duties as assigned. Education and Experience: Required: M.D. Ph.D., Pharm. D., MPH, MSN or RN with 8-10 years industry related experience with a minimum 3-5 years of clinical research experience in clinical development within a biopharmaceutical company. Working knowledge of FDA and EMA regulations and expectations, Good Clinical Practice, ICH guidelines, and clinical drug development. Practical knowledge of the day-to-day medical monitoring of clinical trials required (e.g., review of safety parameters, etc.). Great analytical skills and a passion for “search and find” among complex data generated in clinical studies. Collaborative, effective skills, with the ability to build and maintain strong interpersonal relationships, gaining trust and confidence from all levels within the organization. Ability to inspire and earn respect of the leadership team, colleagues, and staff. Respectful of the ideas and experience of all members of the Crinetics team Ethical, with highest standards of integrity recognizing that we are the creators of hope for our patients and the health care professionals who serve them as well as stewards of the investments of all our shareholders Software Knowledge: Windows, MS Office (Outlook, Word, Excel, PowerPoint). Physical Demands and Work Environment: Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. The noise level in the work environment is typically low to moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions and