Associate Director, Clinical Data Management
About The Position
Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. The Associate Director, Clinical Data Management Leads clinical data management activities across one or more clinical programs, ensuring the timely delivery of high-quality, audit-ready clinical trial data in support of regulatory submissions and clinical development timelines. Acts as the primary data management point of contact for assigned programs, overseeing CRO and vendor performance, database design, and data cleaning strategy from study start-up through database lock. Partners closely with Biostatistics, Statistical Programming, Clinical Operations, Clinical Development, Pharmacovigilance and Quality to ensure data management deliverables align with study milestones, data quality objectives and inspection-readiness standards. This role combines deep technical data management expertise with the leadership skills needed to guide cross-functional teams and external vendors toward consistent, high-quality outcomes. This role reports to the Director, Clinical Data Management.
Requirements
- Bachelor’s degree in Life Sciences, Health Sciences, Computer Science, or a related discipline, or equivalent education and experience.
- Minimum of 7 years of progressive experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry.
- Proven experience managing CDM activities across all phases of clinical development (Phase I–III), including late-stage and/or registration-enabling trials.
- Prior experience managing CRO relationships and overseeing outsourced CDM activities
- Proficiency with EDC platforms (e.g., Medidata Rave, Veeva Vault EDC) and CDISC (CDASH/SDTM/ADaM) standards.
- Working knowledge of data cleaning, query management, and database lock processes.
- Proficiency in medical coding dictionaries (MedDRA, WHO Drug) and coding conventions.
- Familiarity with centralized data review methodologies such as data visualizations and review tools for identifying data quality trends and leveraging risk-based monitoring (RBM) approaches.
- Ability to lead cross-functional study teams and manage CRO performance without direct reporting authority.
- Strong written and verbal communication for cross-functional and vendor collaboration.
- Ability to present data management status and risks to program leadership.
- Skilled at translating technical data issues into clear, actionable summaries for non-DM stakeholders.
- Effective at facilitating technical system design discussions and data quality oversight review meetings with internal and external cross-functional team members
Nice To Haves
- Experience in immunology or autoimmune therapeutic areas preferred
- Strong understanding of CDISC standards CDASH/SDTM, statistical analysis dataset specifications, and submission-ready data packages.
Responsibilities
- Oversee the development and review of key data management study documents such as Data Management Plans, CRF/eCRF design specifications, data validation plans, custom listings/reports, and data cleaning plans.
- Oversee EDC and other clinical data systems build in support of protocol objectives, site-level and patient-level data entry workflows, user acceptance testing (UAT), database releases, mid-study updates, interim snapshots and database lock activities.
- Monitor clinical data quality, study metrics and KPIs to ensure timely and accurate data cleaning, discrepancy management, medical coding (MedDRA, WHO Drug), and reconciliation of external data sources (e.g., central labs, eCOA, safety data).
- Contribute to internal and external cross-functional study team meetings by communicating study status, proactively identifying risks to timelines, data quality, and regulatory compliance, and recommending mitigation strategies.
- Ensure all data management activities comply with ICH E6(R3) GCP guidelines, 21 CFR Parts 11 and 312, data security, privacy (e.g., GDPR, HIPAA) and other applicable global regulatory requirements.
- Contribute to process improvement initiatives, SOP development, and data management standards across programs.
- Support preparation for regulatory inspections and audits by maintaining complete documentation of data management activities and sponsor oversight and ensure regular documentation filings into the Trial Master File.
- Perform other duties and responsibilities as assigned
Benefits
- Competitive health and wellness coverage (structure and premiums vary by country)
- Paid time off, public holidays, and additional leave entitlements in accordance with local requirements
- Flexible work arrangements / hybrid schedule
- A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.
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What This Job Offers
Job Type
Full-time
Career Level
Manager
