Meet Life Sciences is representing a clinical-stage oncology biotech seeking a Medical Director ... Review safety data, participate in data monitoring activities, and act as the primary medical ...
53 Meet Life Sciences Director Data Management Jobs Hiring Near You
Meet Life Sciences is representing a clinical-stage oncology biotech seeking a Medical Director ... Review safety data, participate in data monitoring activities, and act as the primary medical ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
Meet Life Sciences is partnering with a biotech pioneering a novel asset targeting solid tumor ... Review safety data, support data monitoring activities, and act as a primary medical contact for ...
Meet Life Sciences is partnering with a biotech pioneering a novel asset targeting solid tumor ... Review safety data, support data monitoring activities, and act as a primary medical contact for ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
... meet regulatory requirements, internal standards, and industry best practices * Manage external ... PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required * 8+ ...
Strong understanding of PK, PD, biomarker, and immunogenicity data * Experience working in cross ... Strong scientific writing and documentation skills under GxP standards * Ability to manage multiple ...
Strong understanding of PK, PD, biomarker, and immunogenicity data * Experience working in cross ... Strong scientific writing and documentation skills under GxP standards * Ability to manage multiple ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
Strong understanding of PK, PD, biomarker, and immunogenicity data * Experience working in cross ... Strong scientific writing and documentation skills under GxP standards * Ability to manage multiple ...
Strong understanding of PK, PD, biomarker, and immunogenicity data * Experience working in cross ... Strong scientific writing and documentation skills under GxP standards * Ability to manage multiple ...
Strong understanding of PK, PD, biomarker, and immunogenicity data * Experience working in cross ... Strong scientific writing and documentation skills under GxP standards * Ability to manage multiple ...
Strong understanding of PK, PD, biomarker, and immunogenicity data * Experience working in cross ... Strong scientific writing and documentation skills under GxP standards * Ability to manage multiple ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
... science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical ... and data interpretation • Partner cross-functionally with regulatory, translational, and ...
Meet Life Sciences Jobs Information
What are the key skills and qualifications needed to thrive as a Director of Data Management, and why are they important?
What are some common challenges faced by a Director of Data Management when implementing data governance frameworks?
What is a Director of Data Management?
What is the difference between Director Data Management vs Data Analyst?
| Aspect | Director Data Management | Data Analyst |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Data Science, IT, or related field; often with leadership experience | Bachelor's in Statistics, Data Science, or related field; often entry to mid-level experience |
| Work Environment | Strategic leadership, overseeing data teams, managing data governance | Data collection, analysis, reporting, supporting decision-making |
| Employer & Industry Usage | Used in large corporations, tech, finance, healthcare | Common across industries for data-driven roles |
The main difference is that a Director Data Management focuses on strategic oversight, data governance, and leading data teams, while a Data Analyst primarily handles data analysis, reporting, and supporting business decisions. The Director role involves higher-level management and planning, whereas Data Analysts execute specific data tasks.

Full-time
Posted 28 days ago
Job description
Meet Life Sciences is representing a clinical-stage oncology biotech seeking a Medical Director / Senior Medical Director to support the clinical development of oncology programs. This role will focus on the design, execution, and oversight of clinical trials, including contributing to clinical strategy, serving as primary Medical Monitor, supporting regulatory submissions, and collaborating with cross-functional teams. The position will provide scientific and medical input to ensure the successful conduct of clinical trials and advancement of oncology assets.
This role reports to the VP, Clinical Development, Oncology and is based in our client's Cambridge, MA office. This role would require a candidate to work on-site 3 times per week.
Key Responsibilities
- Clinical Trial Support: Provide medical expertise to support the lead physician/scientist in the design and execution of oncology clinical trials. Collaborate with clinical operations to ensure trials are conducted in alignment with scientific objectives, patient safety standards, and regulatory requirements.
- Medical Monitoring: Serve as Medical Monitor for assigned clinical trials, ensuring patient safety, protocol compliance, and medical oversight. Review safety data, participate in data monitoring activities, and act as the primary medical contact for study teams and investigators.
- Cross-functional Collaboration: Partner with regulatory affairs, clinical operations, pharmacovigilance, biostatistics, medical affairs, and commercial teams to align clinical and business objectives, often across multiple time zones.
- External Representation: Represent our client in interactions with investigators, key opinion leaders, regulatory authorities, and external collaborators.
- Data Analysis & Interpretation: Analyze clinical trial data and real-world evidence to identify trends, assess efficacy and safety signals, and support data-driven decision-making. Collaborate with cross-functional teams to translate findings into actionable insights that inform clinical strategy, regulatory submissions, and program advancement.
- Regulatory Support: Support the preparation of regulatory documents, participate in health authority interactions, and contribute to risk management planning and mitigation strategies throughout the development lifecycle.
- Business Development Support: Support the medical leadership team with licensing opportunities, partnerships, and due diligence activities.
- Scientific Support: Maintain up-to-date knowledge of oncology trends, the competitive landscape, and regulatory changes to inform clinical strategy and contribute to the clinical development function.
Qualifications
Required
- MD with board certification in Oncology, Hematology-Oncology, or a related specialty.
Preferred
- Clinical development experience, with a focus on late-stage trials, preferably as a Medical Monitor.
- Experience working in cross-functional team environments.
- Strong understanding of oncology drug development, clinical endpoints, and regulatory pathways.
- Clinical practice experience or experience as an investigator.
- Strong communication skills.
- Effective collaboration skills with the ability to interact with internal and external stakeholders.
- High ethical standards and commitment to scientific rigor.