Senior Clinical Data Manager

Revolution Medicines; San Francisco (CA); On-site; USD 158,000 - 198,000; Full time

Job summary

Join a pioneering company dedicated to precision oncology as a Senior Clinical Data Manager. In this role, you will oversee all data management processes for clinical trials, ensuring the integrity and accuracy of data while collaborating with cross-functional teams. Your expertise will guide the development and implementation of data management plans, and your leadership will support junior team members. This is an exciting opportunity to contribute to groundbreaking therapies for patients with RAS-addicted cancers, all while working in a dynamic and supportive environment. If you are passionate about making a difference in oncology and possess strong data management skills, this role is perfect for you.

Benefits

Competitive cash compensation

Robust equity awards

Strong benefits

Learning and development opportunities

Qualifications

• 3-5 years of Data Management experience in the pharmaceutical industry.
• Solid knowledge of clinical trials process and regulatory requirements.

Responsibilities

• Manage data management timelines and deliverables for clinical trials.
• Review and approve study documents and provide oversight of database set-up.

Skills

Clinical Data Management

Project Management

Regulatory Requirements Knowledge

Technical Skills (EDC, MS Office)

Interpersonal Skills

Organizational Skills

Education

Bachelor’s degree in health sciences or related field

Tools

EDC systems

SAS

Job description

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine data review through database lock of clinical trials. The Sr/CDM has a broad, fundamental knowledge of the data management process and can plan, manage and coordinate all Data Management activities for assigned study(ies) with minimal guidance. This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you will be responsible for:

• Represents data management in study team meetings, able to facilitate and provide data management updates and/or input when appropriate.
• Manages data management timelines to coordinate and synchronize deliverables with the overall study timelines.
• Generates and/or reviews/approves study documents (e.g. Data Management Plans, Case Report Forms, DB build specifications, data transfer specifications, SAE and/or external data reconciliation plans, coding conventions, laboratory data handling plan, study protocols).
• Reviews protocols for appropriate data capture including electronic Case Report Form (eCRF) design and external data vendors’ systems.
• Provides oversight of database set-up/migrations/updates including coordinating and performing UAT.
• Leads the development of internal Data Review Plan and coordinates cross-functional team data listing review.
• Coordinates the internal medical coding review.
• Performs ad hoc and scheduled data listing review and generates/resolves queries in EDC.
• Performs external data reconciliation against EDC.
• Performs Serious AE reconciliation according to SOPs and guidelines, as applicable.
• Executes and/or distributes data management metrics, listings, and reports.
• Provides oversight of data management CRO/service providers including manages and monitors the progress of data management activities with CROs and/or other service providers on assigned studies; build effective relationships with CRO/service provider counterparts.
• Reviews and provides feedback to the clinical team on other study documents e.g., Clinical Monitoring plans and vendor specifications.
• Provides training on the EDC system and/or CRF completion guidelines and EDC system to internal or external study team members, as needed.
• Proactively identifies potential study issues/risks and recommends/implements solutions.
• Maintains study DM related documents/files for inspection readiness.
• Provides DM support to Statisticians and Statistical Programmers in production of clinical trial reports and other deliverables.
• Assists with the training of new employees and/or contractors (e.g., clinical data associates and/or junior clinical data managers working on the studies).
• Participates in CRO/vendor selection process for outsourced activities.
• Supports budget and resource planning across assigned projects.
• Participates in the development, review and implementation of departmental SOPs, templates, and processes.
• Participates in department or cross-functional initiatives (as needed).
• Contributes to a professional working environment through exemplifying RevMed Core Values.

Required Experience, Skills, and Education:

• Bachelor’s degree in health sciences, Life Sciences, Mathematics, Computer Sciences, or health-related field.
• At least three years for CDM and five years for Sr. CDM of Data Management experience in the pharmaceutical or biotechnology industry, depth and exposure to DM related tasks considered in lieu of minimum requirement.
• Requires solid knowledge of clinical data management principles, clinical trials process and regulatory requirements.
• Good working knowledge of ICH, FDA, and GCP regulations and guidelines.
• Strong well-rounded technical skills (EDC systems, MS Word, Excel, PowerPoint).
• Knowledge of industry standards (CDISC, SDTM, CDASH).
• Experience with web-based Electronic Data Capture (EDC), clinical data management systems and industry wide thesauri, such as MedDRA and WHO Drug.
• Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment.
• Ability to handle multiple projects and prioritize effectively, well organized and detail oriented.
• Proven ability to work both independently and in a team setting.

Preferred Skills:

• CRO/Service provider management experience.
• Prior oncology/solid tumor experience highly desired.
• Working knowledge of statistical programming packages (e.g. SAS) is a plus.

The base salary range for this full-time position is $158,000 to $198,000 for candidates working onsite at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the salary for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base salary is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.

Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact [e-mail].