Senior Clinical Scientist

🕒 March 1

🏄 California – Remote

🏄 California – Remote

💵 $180k - $210k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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Crinetics Pharmaceuticals

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2015

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Crinetics Pharmaceuticals is a biotechnology company that develops innovative therapies for endocrine diseases. The company is focused on addressing unmet medical needs by creating treatments for conditions such as acromegaly, carcinoid syndrome, ACTH-dependent Cushing’s syndrome, congenital adrenal hyperplasia, and other endocrine disorders. Crinetics is committed to improving the quality of life for patients through cutting-edge science and robust clinical trials. Their pipeline includes promising candidates like paltusotine, which has been accepted by the U. S. Food and Drug Administration for the treatment of adult patients with acromegaly. The company collaborates with healthcare practitioners and stakeholders to ensure that their therapies address real-life problems effectively and build value for investors by entering market niches with significant needs.

📋 Description

• Provide clinical expertise and scientific insights to help monitor, track, and analyze subjects’ data in phase 1 - 3 studies • Collaborate with the Medical Lead and groups involved in Clinical Development such as Pharmacokinetics, Clinical operations, Biometrics, Pharmacovigilance, and Medical Affairs • Monitor, analyze, and review safety and efficacy data for events of interest • Review laboratory parameters, patient profiles, data listings, summary tables • Collaborate with clinical leads and medical directors on scientific content and program strategy • Support authoring and review of various clinical and regulatory documents • Address scientific and protocol related issues from investigators • Contribute to safety narratives, manuscripts, and scientific presentations • Support preparation for safety review committees • Review protocol deviations to identify cause and resolution • Participate in Database lock activities and represent CR at internal meetings • Contribute to the development of regulatory documents in collaboration with Medical Affairs and Patient Advocacy • Participate in research site identification and relationship building with CROs

🎯 Requirements

• M.D., Ph.D., Pharm. D., MPH, MSN or RN with 8-10 years industry related experience • 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 • 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 • 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 they are the creators of hope for patients and healthcare professionals.

🏖️ Benefits

• Health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance • 20 days of PTO • 10 paid holidays • Winter company shutdown • Discretionary annual target bonus • Stock options • ESPP • 401k match