Top 6 Biostats & Programming Jobs

Manager Clinical Data
Monte Rosa Therapeutics, Inc —Boston, MA
- $115,000 - $145,000 a year
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
Director, Early Phase Biostatistics
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $201,840 - $302,760 a year
- 7 years
- Doctor of Philosophy
- Travel
Senior Director, Biostatistics Oncology
Ipsen Biopharmaceuticals Inc. —Cambridge, MA
- Full-time
- English
- Doctor of Philosophy
- Quality control
Associate Director, Biostatistics
Gilead Sciences —Foster City, CA
- $177,905 - $253,220 a year
- Full-time
- 5 years
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Principal Biostatistician
Biogen —Cambridge, MA
- $123,000 - $163,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Presentation skills
- Doctor of Philosophy
- Paid parental leave
- Employee stock purchase plan
EDC Programmer
CG Oncology Inc —Remote
- $115,000 - $135,000 a year
- Full-time
- Remote
- Computer Science
- 5 years
- System design
- Health savings account
- Disability insurance
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Manager Clinical Data

Monte Rosa Therapeutics, Inc
Boston, MA

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Job Details

Full-time
$115,000 - $145,000 a year

Qualifications

Vendor relationship building
ICH guidelines
Vendor relationship management
Cross-functional collaboration
Cross-functional communication

Full Job Description

Overview:

The Manager, Data Management will be responsible for overseeing clinical data management activities across one or more clinical programs. This individual will work closely with Clinical Operations, Biostats and Programming, Medical, Safety, Regulatory, external CROs, and technology vendors to ensure high-quality, inspection-ready clinical data.

This is a hands-on role well suited for someone who thrives in a small biotech environment, can manage external partners effectively, and is comfortable moving between strategy, execution, and problem-solving.

Responsibilities:

Oversee end-to-end clinical data management activities for assigned studies, from study start-up through database lock.
Manage CROs, EDC vendors, central labs, imaging vendors, eCOA providers, IRT vendors, and other data providers.
Review and contribute to key study documents, including data management plans, edit check specifications, CRF completion guidelines, data transfer agreements, and data review plans.
Support CRF design, database build, user acceptance testing, and EDC system validation activities.
Ensure timely data cleaning, query management, reconciliation, coding, and database lock activities.
Coordinate external data transfers and reconciliations, including laboratory, pharmacokinetic, biomarker, imaging, safety, and IRT data.
Partner with Clinical Operations and study teams to identify data quality issues and drive resolution.
Support medical coding activities using MedDRA and WHODrug, as applicable.
Contribute to clinical data review meetings and help prepare data outputs for internal decision-making.
Maintain data management documentation in compliance with GCP, ICH guidelines, SOPs, and regulatory expectations.
Support vendor selection, budget review, timelines, performance oversight, and issue escalation.
Contribute to process development and continuous improvement as the company scales its clinical operations infrastructure.

Qualifications:

BS/MS degree in life sciences, data sciences, health sciences, or a related field.
8+ years of clinical data management experience in biotech, pharmaceutical, CRO, or related clinical research settings.
Experience supporting oncology and/or immune disease clinical trials.
Strong working knowledge of EDC systems such as Medidata Rave or similar platforms.
Experience managing CROs and external clinical data vendors.
Familiarity with clinical trial data standards, including CDISC, SDTM concepts, and database lock processes.
Understanding of GCP, ICH guidelines, regulatory requirements, and clinical trial documentation standards.
Strong attention to detail, organizational skills, and ability to manage multiple priorities in a fast-paced environment.
Excellent communication and cross-functional collaboration skills.
Experience in a small biotech or emerging pharmaceutical company.
Experience with early-phase oncology trials, dose escalation, expansion cohorts, and complex biomarker-driven studies.
Familiarity with molecularly targeted therapies, protein degradation, or immune-mediated disease programs.
Experience with external data types such as genomics, biomarkers, PK/PD, central imaging, and specialty labs.

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Biostats & Programming jobs

Manager Clinical Data

Director, Early Phase Biostatistics

Senior Director, Biostatistics Oncology

Associate Director, Biostatistics

Principal Biostatistician

EDC Programmer

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