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Senior Manager, Clinical Data Management

10 May 5, 2025
Job Description
Job Type: Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Senior Manager, Clinical Data Management

Company: Eikon Therapeutics
Location: Jersey City, NJ / New York, NY / Millbrae, CA (Hybrid – minimum 3 days onsite/week)


Job Type: Full-time

Salary Range: $152,000 – $166,250 (plus bonus & equity)


About the Company

Eikon Therapeutics is a cutting-edge biopharmaceutical company leveraging Nobel Prize-winning imaging technology to track protein movement in living cells, opening new doors in drug discovery for life-threatening diseases.


Role Summary

The Senior Manager, Clinical Data Management will lead end-to-end data management activities for clinical trials, ensuring data quality, compliance, and readiness for regulatory submissions. This position serves as a key interface between internal teams and external vendors and plays a central role in driving data strategy across Eikon’s development programs.


Key Responsibilities

  • Lead data management for one or more clinical programs across multiple phases

  • Serve as the primary DM point of contact for internal teams and external vendors

  • Oversee third-party vendors ensuring quality and timeliness of DM deliverables

  • Create/review study documents: DQMP, DVP, DRP, eCRF guidelines, etc.

  • Manage EDC systems (preferably Veeva CDMS), eCOA, RTSM, and other data tools

  • Lead data review meetings, audits, and support regulatory inspections

  • Provide oversight and mentoring to junior DM staff

  • Ensure adherence to CDISC/CDASH standards and submission requirements

  • Contribute to development/validation of standard eCRF library

  • Represent Data Management on cross-functional study and submission teams


Qualifications

  • Master’s degree with 6+ years or Bachelor’s degree with 8+ years of experience in Life Sciences, Biostatistics, or related field

  • Strong experience across full clinical trial lifecycle, ideally with CROs and sponsors

  • Oncology clinical trial experience is required

  • Expertise in FDA/ICH regulatory standards and CDISC/CDASH implementation

  • Deep experience with EDC platforms, particularly Veeva CDMS

  • Strong project management, communication, and cross-functional collaboration skills

  • Understanding of regulatory submission processes (e.g., NDA, BLA, MAA)


Compensation & Benefits

  • Competitive base salary, bonus, and equity awards

  • 401(k) with company match

  • Medical (95%), dental & vision (100%) premiums fully covered

  • Mental health and wellness programs

  • Generous PTO and paid holidays

  • Weeklong summer and winter shutdowns

  • Life/AD&D insurance fully covered + optional supplemental coverage

  • Enhanced parental leave

  • Daily subsidized lunch program onsite


Diversity & Inclusion

Eikon Therapeutics is proud to be an equal opportunity employer. All qualified applicants will receive consideration without regard to race, gender, disability, or veteran status.