Crinetics Pharmaceuticals
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.
Drug Discovery • Endocrinology • RareDisease • Biotech
Director, Medical Writing
March 15
Crinetics Pharmaceuticals
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.
Drug Discovery • Endocrinology • RareDisease • Biotech
📋 Description
• Overseeing and managing the scientific medical writing group • Ensuring adequate resources for document development • Writing, review, and approval of clinical and regulatory documents • Collaborating across functions for document development activities • Instituting improvements to department operations
🎯 Requirements
• Bachelor’s degree • Minimum 12 years of regulatory medical writing experience in the biotech/pharmaceutical industry • Minimum 8 years in a leadership role • Experience writing sections of INDs/BLAs/NDAs/MAAs • Understanding of CTD structure and granularity requirements • Extensive experience with clinical protocols and clinical study reports • Proficient with electronic document management systems • Knowledge of relevant medical writing regulations • Ability to manage multiple writing projects • Strong written and verbal communication skills • Excellent standard of written English
🏖️ Benefits
• Discretionary annual target bonus • Stock options • Employee Stock Purchase Plan (ESPP) • 401k match • Top-notch health insurance plans (medical, dental, vision, and basic life insurance) for employees and their families • 20 days of PTO • 10 paid holidays • Winter company shutdown
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