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Genomic Program Manager Jobs in Lexington, MA (NOW HIRING)

Socket.dev

Senior Director, Multiomics

Boston, MA · On-site

$250 - $400/hr

General Manager, Ginkgo Datapoints Focus: Scientific Excellence, Commercial Strategy (P&L ... The role is anchored in discovery-stage functional genomics, with real room to extend our multiomic ...

ZS

Bioinformatics Leader

Boston, MA · On-site

$200K - $229K/yr

As a management consulting and technology firm focused on improving life and how we live it, we ... Design and implement computational workflows for analysis of multi-omic data (genomics ...

LGC Biosearch Technologies

Account Manager

Milford, MA · On-site

$105K/yr

Competitive compensation with strong bonus program * Comprehensive medical, dental, and vision ... Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and ...

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All JobsGenomic Program JobsGenomic Program Manager JobsGenomic Program Manager Jobs in Lexington, MA

Genomic Program Manager information

See Lexington, MA salary details

$43.3K

$120.7K

$176.4K

How much do genomic program manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for genomic program manager in Lexington, MA is $120,736.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,300.00 and $148,900.00 per year, depending on experience, location, and employer.

What is a genomic program manager?

Genomic Program Managers are professionals who oversee and coordinate projects related to genomics, such as research studies, clinical trials, or implementation of genomic technologies. They are responsible for planning, managing resources, ensuring compliance with regulations, and facilitating communication among multidisciplinary teams. Their role bridges the gap between scientific research and operational execution, ensuring that genomic initiatives are delivered efficiently and effectively.

What are the key skills and qualifications needed to thrive as a genomic program manager?

To thrive as a Genomic Program Manager, you need expertise in genomics or genetics, program management experience, and typically an advanced degree in life sciences or a related field. Familiarity with bioinformatics tools, data analysis platforms, and regulatory compliance systems is often required. Strong leadership, communication, and stakeholder management skills help drive cross-functional collaboration and project success. These capabilities ensure effective coordination of complex genomic projects, alignment with scientific objectives, and successful delivery of program outcomes.

How does a genomic program manager typically collaborate with cross-disciplinary teams to ensure successful project outcomes?

A Genomic Program Manager routinely partners with scientists, bioinformaticians, clinicians, and data analysts to coordinate complex projects involving genomic data. They act as a bridge between different stakeholders, facilitating communication, aligning project goals, and ensuring that deliverables are met on time. Regular meetings, progress tracking, and clear documentation are essential aspects of this collaboration. By fostering a cohesive team environment and addressing any interdisciplinary challenges, the Program Manager helps ensure that projects advance efficiently and according to regulatory and scientific standards.

What job categories do people searching Genomic Program Manager jobs in Lexington, MA look for?

The top searched job categories for Genomic Program Manager jobs in Lexington, MA are:

Genomic Program Manager jobs near you
Infographic showing various Genomic Program Manager job openings in Lexington, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 85% In-person, and 15% Remote job distribution, with an average salary of $120,736 per year, or $58 per hour.

Manager Clinical Data

Monte Rosa Therapeutics, Inc

Boston, MA • On-site

$115K - $145K/yr

Full-time

Re-posted 8 days ago

Job description

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.


  • 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.

  • 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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