Senior Clinical Data Manager (CDM)

W2 Contract

Pay Rate: $80 - $90 per hour

Location: South San Francisco, CA - Remote Role

Job Summary:

In anticipation of the Company's growth plans, we are seeking to recruit a Senior Clinical Data Manager (CDM) Contractor. The Senior CDM Contractor will work in an outsourced data management model. He or she will develop a strategy, lead data management activities, and interface with the project team to ensure that data management services are delivered in a consistent, high-quality manner. This individual will also independently perform/oversee tasks related to database and report setup, as well as processing and cleaning clinical trial data, following all applicable standards and study-specific procedures.

Duties and Responsibilities:

• Serve as a data management expert and, if assigned, be the CDM Lead for assigned clinical studies on multidisciplinary project teams.
• Deliver high-quality data for analysis and study milestones.
• Review protocols from a CDM perspective and provide functional-expert feedback.
• Review and approve key clinical data management deliverables generated by a DM vendor, including: Case Report Form (CRF) design, CRF completion guidelines, database design specifications, data entry guidelines, data management plans, edit check specifications, serious adverse event reconciliation plans, medical coding, data listing specifications, and electronic data transfer agreements.
• Manage/oversee study setup, testing, and system validation for new studies in partnership with the DM vendor.
• Oversee data cleaning activities executed by the DM vendor and ensure protocol-specified guidelines are applied to the review and cleaning of clinical data.
• Collaborate with internal Data Science (statistical programming), internal Biostatistics, and internal Medical Monitor on identifying critical variables in the clinical dataset for protocol-specified endpoints. Coordinate implementing these variables into DM vendor activities.
• Develop and manage timelines for key clinical data management deliverables in coordination with the clinical data management vendor and our project team.
• Monitor vendor performance to ensure timelines and data quality standards are met.
• Ensure compliance of clinical data management processes with applicable regulations and guidelines.

Requirements and Qualifications:

• Typically requires a Bachelor's degree in mathematics, science, or a health-related field and a minimum of 10 years of clinical data management experience in biotech, pharmaceutical, or health-related industries.
• Demonstrated proficiency leading CDM deliverables across Phase 1–3 clinical trials, including early-phase and dose-escalation studies
• Solid understanding of the clinical drug development process and regulatory/data standards (ICH/FDA, CDISC - CDASH, SDTM, ADaM - GCDMP, 21 CFR Part 11, MedDRA, WHO Drug Dictionaries, GDPR)
• Demonstrated understanding of the clinical trial database life cycle, including CRF design, development/testing, discrepancy management, data quality review, and database lock
• Capable of proactively identifying project risks and proposing strategic solutions; excellent multidisciplinary interpersonal and communication skills
• Strong analytical and problem-solving skills; able to work independently and within cross-functional project teams

Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate. 

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