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Precision Medicine GroupPrincipal/Senior Clinical Data Scientist
Precision Medicine Group is hiring a Principal or Senior Clinical Data Scientist to head up the clinical science division for oncology, rare diseases, and autoimmune clinical…
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About This Role
Precision Medicine Group is hiring a Principal or Senior Clinical Data Scientist to head up the clinical science division for oncology, rare diseases, and autoimmune clinical development programs. This position spans the entire lifecycle of a trial, starting from initial setup up to database lock, ensuring that projects remain aligned with quality benchmarks, schedules, and financial scopes. The person in this role will act as a scientific subject matter expert,…
Job Description
Precision Medicine Group is hiring a Principal or Senior Clinical Data Scientist to head up the clinical science division for oncology, rare diseases, and autoimmune clinical development programs. This position spans the entire lifecycle of a trial, starting from initial setup up to database lock, ensuring that projects remain aligned with quality benchmarks, schedules, and financial scopes.
The person in this role will act as a scientific subject matter expert, guiding electronic case report form designs, validation processes, edit checks, and ongoing data cleaning. Responsibilities include performing detailed individual and aggregate participant data reviews utilizing various software platforms, collaborating with medical monitors, and participating in risk-based quality management meetings. This position also involves supporting project management invoicing, training junior team members, maintaining trial master file documents, and aiding business development efforts during bid defense presentations.
Ideal candidates possess extensive backgrounds in clinical research with a strong concentration in oncology, paired with leadership experience and a strong grasp of medical terminology and regulatory standards.
Responsibilities
- Manage the clinical science functional scope on assigned oncology, rare diseases, and autoimmune projects from startup through database lock.
- Conduct holistic individual and aggregate participant data reviews utilizing proprietary and non-proprietary data review tools.
- Guide electronic case report form design, data capture requirements, edit checks, and completion guidelines.
- Support risk-based quality management by identifying study risks and participating in review meetings.
- Collaborate with medical monitors to oversee data review findings and provide operational protocol reviews.
- Oversee or develop clinical science project plans, guidelines, trackers, and programming specifications.
- Facilitate medical data review meetings and participate in internal and external team presentations.
- Support business development needs, including bid defense meeting attendance and presentations.
Requirements
- Bachelor degree or equivalent combination of education and experience in a science or health-related discipline.
- Minimum of 8 years of clinical research experience.
- Minimum of 3 years of oncology experience acquired within the past 1.5 years.
- Minimum of 1 year of leadership experience.
- High proficiency with Microsoft Office products.
- Professional proficiency in written and oral English.
- Ability to occasionally travel domestically and internationally with overnight stays up to 25%.
Qualifications
- Medical-related degree such as RN, OCN, RPh, or PharmD.
- Experience with electronic data capture systems and database build.
- On-site experience as a nurse or study coordinator, or experience in clinical monitoring and data review.
- Familiarity with data visualization platforms or software.
- Experience working on phase I, II, and III studies as well as global clinical trials.
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
What is the employment type for this role?
The posting lists the employment type as full-time.
Is remote work permitted for this position?
The source posting mentions the ability to work remotely while independently leading and supporting tasks, but does not specify a formal remote or hybrid policy beyond noting occasional domestic and international travel up to approximately 25%.
What is the salary or compensation offered?
The salary is not stated in the job posting.
What are the core experience prerequisites?
Applicants must have at least 8 years of clinical research experience, including a minimum of 3 years of oncology experience gained within the past 1.5 years, and at least 1 year of leadership experience.
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