
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.
🕒 February 19
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Ensure company compliance with clinical trial transparency laws and requirements by applying expert knowledge of key regulatory frameworks, including FDAA 801 and Final Rule and CTR 536/2014 • Work with cross-functional teams to develop content for clinical trial and results postings and post all approved materials in accordance with regulations • Develop and implement internal procedures, processes, templates, and tools for all aspects of clinical trial disclosure • Develop and maintains CCI documents (process owner) • Prepare redacted documents for postings ensuring CCI and personal protected information (PPI) in accordance with the General Data Protection Regulation in the EU and other privacy laws are identified for redaction and redacted from documents that are posted publicly • Apply logic, attention to detail, critical thinking, good judgement, and follow-up skills to every deliverable and situation • Approach all engagements with cross-functional team members with a customer-service mindset • Other duties as assigned
• Bachelor’s Degree required; advanced degree in life sciences, public health, regulatory science, or related discipline preferred (eg, MS, MPH, PharmD, PhD) • 7-years’ experience in Trial Disclosure desired with flexibility of combined experience in closely related industry field with some responsibility for disclosure and results reporting activities (eg, clinical operations or regulatory affairs) • Experience managing CT.gov on behalf of an organization, including ensuring regulatory timelines are met for trial disclosure and results reporting • Experience posting trial results to CTIS in accordance with regulatory timelines • Demonstrated experience independently translating clinical protocols into accurate disclosure postings and interpreting clinical study reports to create accurate results postings within the parameters of the disclosure platform (eg, CT.gov, CTIS) • Experience developing/managing process for development, review and approval of documents with redacted (red box and black box) company confidential information and personally identifiable information • Demonstrated ability to collaborate across functional scientific and operational disciplines to drive alignment on process and content • Strong project management skills with ability to manage multiple projects with overlapping timelines while adhering to regulatory requirements for each individual deliverable • Experience with controlled electronic document management systems • Ability and adaptability to incorporate existing or new technologies to automate current manual processes • Excellent verbal and written communication skills in English • Experience as process owner for development and maintenance of company confidential information documentation preferred.
• discretionary annual target bonus • stock options • ESPP • 401k match • top-notch 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
Apply Now🕒 January 14
201 - 500
GenAI Creative Prompt Writer crafting context-rich prompts for diverse policy domains. Blending linguistic creativity with sociocultural insights for AI models in various contexts.
🕒 January 8
Writing Specialist crafting and refining elite-level writing across various genres. Collaborating with engineers and other specialists to enhance AI's writing capabilities at xAI.
🇺🇸 United States – Remote
💵 $40 - $125 / hour
💰 $10M Series B on 2017-08
⏰ Full Time
🟡 Mid-level
🟠 Senior
✏️ Content Writer
🕒 December 1, 2025
Content Writer developing and maintaining the brand voice for Duna's digital platforms. Creating compelling content in a fast-moving remote-first environment.
🕒 November 1, 2025
11 - 50
Senior Product Marketing Manager bringing to market a new writing application for academic integrity. Collaborating with sales and marketing teams for product launch, user adoption, and success.
🕒 October 24, 2025
Proposal Writer developing IT proposals for federal government RFPs and RFIs. Collaborating with team members and subject matter experts for technical accuracy.