Director, Clinical Data Management

to lead study-level data management activities in support of our oncology clinical development programs. This individual will serve as the compound CDM lead for one or more clinical trials, responsible for the planning, execution, and oversight of data management activities in collaboration with internal stakeholders, including US/ex-US DM team and external partners (e.g., CROs, technology vendors). This is an exceptional opportunity to contribute directly to the success of high-impact oncology trials in a dynamic and collaborative environment. The role will report to the Head of Clinical Data Management and may evolve to include line management responsibilities as the organization grows. You will be responsible for…

Study-Level Data Management

Serve as the primary data management lead for assigned clinical trials, ensuring timely,

high-quality data deliverables

throughout the data lifecycle. Develop and maintain study-specific

data management plans (DMPs)

and associated documents such as CRF completion guidelines, edit check specifications, and data transfer specifications. Oversee

case report form (CRF) design , eCRF programming, and database setup activities in coordination with CRO partners and internal stakeholders. Coordinate and perform

data review , query management, and data cleaning activities; support interim and final

database lock processes . Ensure that data management practices are consistent with applicable regulatory requirements (e.g., ICH GCP, FDA) and industry best practices (e.g. GCDMP). Support the integration and reconciliation of

external data sources , including central labs, imaging, biomarker, and other third-party data providers. Cross-Functional Collaboration

Work closely with Clinical Operations, Biostatistics, Medical, and Regulatory Affairs to align trial objectives, timelines, and data expectations. Act as the

data management point-of-contact

during study planning, conduct, and closeout phases. Lead Data Working Groups and

cross-functional data review meetings

to ensure data quality is maintained throughout the study. Contribute to the development of

clinical trial protocols

and statistical analysis plans (SAPs) from a data management perspective. Functional Vendor Oversight

Collaborate with and provide

oversight of NUVB ex-US DM collaborators, CROs and third-party vendors , ensuring the quality and timeliness of deliverables. Participate in vendor selection and contracting activities; contribute to the development of vendor performance metrics. Ensure effective communication between vendors and internal teams to proactively address data-related issues. Process and Quality Support

Contribute to the development and continuous improvement of

data management processes, SOPs, and standards

within the organization. Support regulatory inspections and audits by providing documentation and subject matter expertise as needed. May lead or participate in

data-focused initiatives , such as implementing new data review tools and R shiny apps, standardizing data review workflows, or adopting novel data sources (e.g., ePRO, wearables). Team Leadership

As the team grows, may provide

mentorship or line management

to junior CDM staff or contractors. Participate in training, onboarding, and professional development of new team members What Knowledge & Experience you’ll bring to us…

Bachelor’s degree

in life sciences, data science/statistics/math, computer science, health informatics, or related field required;

advanced degree

preferred. 8+ years

of clinical data management experience in the biotech, pharmaceutical, or CRO industry. 3+ years

of experience

managing people, vendors, and functional teams . Strong leadership, strategic thinking, and communication skills Strong working knowledge of

clinical data systems (preferably Medidata Rave)

and

CDISC standards (SDTM, CDASH) . Experience managing

third-party vendors

and overseeing outsourced data management activities. Thorough understanding of

GCP, ICH, and relevant regulatory guidelines . Comfortable working in a

fast-paced, hands-on environment

with the ability to pivot as priorities evolve. Prior experience working in a

small biotech

or startup environment is highly desirable. Familiarity with

complex data types

(e.g., imaging, genomics, digital endpoints) in oncology trials is desirable. Demonstrated ability to balance

strategic thinking with hands-on execution . Experience supporting

regulatory submissions

(e.g., NDA, BLA) is a plus. Behavioral skills to be successful…

Problem-Solver

• As an action-oriented self-starter, you’re eager to apply your expertise in diagnosing inefficiencies, determining root causes, and recommending solutions to complex challenges. Personable

• You establish and nurture highly effective relationships with colleagues and key stakeholders that support and advance project goals and objectives. Credible

• Thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource. Emotional intelligence , curiosity, and a knack to figure out a way to build something better Communication

• Effectively listens, conveys, and receives ideas. Maintains a consistent flow of information. A strong presenter and effective communicator with the ability to influence stakeholders. Accountability

• Acts with a clear sense of ownership - whether the task is in their role description. Holds yourself and others accountable to execute all tasks at hand through seen and unforeseen circumstances with high quality and integrity. Adaptability

• Can manage in an environment of ambiguity. Embraces the change of a new system, process, technology, or idea in the organization. You could reassess priorities, alter goals and take risks. What we have for you!

Competitive Base Salary, Bonus, and Equity Plans Unlimited Vacation and 10 Sick Days Annually Excellent Medical, Dental, and Vision Coverage 401K with Company Matching and much more! The base pay offered will take into account internal equity and also may vary depending on the candidate’s job-related knowledge, skills, experience, and location among other factors. Our full-time regular positions also include an annual performance-based bonus and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, depending on the level and position offered. Disclaimer

Nuvation Bio is a biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates. Our vision is to significantly change the practice of oncology by developing medicines that provide truly meaningful improvements in quality of life and survival for people with cancer. What you’ll be doing