Manager, Trial Disclosure, Medical Writing Operations
Crinetics Pharmaceuticals
full-time
Posted on:
Location Type: Remote
Location: California • United States
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Salary
💰 $130,000 - $154,000 per year
About the role
- 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
Requirements
- 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.
Benefits
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial transparencyregulatory frameworksFDAA 801Final RuleCTR 536/2014clinical trial disclosureCT.govCTISdocument redactionclinical protocols
Soft Skills
attention to detailcritical thinkinggood judgementfollow-up skillscustomer-service mindsetcollaborationproject managementadaptabilityverbal communicationwritten communication
Certifications
Bachelor’s DegreeMSMPHPharmDPhD