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Edc Project Manager Jobs in Cambridge, MA (NOW HIRING)

ARTBIO

Senior Director, Clinical Operations

Cambridge, MA · On-site

$120 - $160/hr

... project management, regulatory, quality, finance, and translational and discovery research, to ... Experience with study tools, including CTMS, eTMF, Medidata RAVE, and other EDC systems. EEO ...

Care Access

Central Study Coordinator I

Boston, MA · Hybrid

The CSC also serves as a project manager for their assigned studies with their assigned PIs ... Enter data and resolve queries in EDC and other portals within appropriate time window defined by ...

Tango Therapeutics

Site Management Leader (SML)

Boston, MA · On-site

$128K - $192K/yr

Familiarity with clinical trial systems (e.g., CTMS, eTMF, EDC, IRT, eCOA) and operational metrics, KPIs, and KRIs * Strong vendor management and project management skills * Leadership skills with ...

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All JobsEdc Project JobsEdc Project Manager JobsEdc Project Manager Jobs in Cambridge, MA

Edc Project Manager information

See Cambridge, MA salary details

$42.1K

$112.2K

$177.1K

How much do edc project manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for edc project manager in Cambridge, MA is $112,229.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,800.00 and $134,400.00 per year, depending on experience, location, and employer.

Does Edc Project Manager offer remote work options?

The Edc Project Manager role may offer remote work options depending on the employer's policies. Many project management positions can be performed remotely, especially with skills in collaboration tools and virtual communication. Candidates should verify specific job postings for remote work availability.

What are some common challenges faced by EDC project managers when implementing new electronic data capture systems?

EDC Project Managers often encounter challenges such as ensuring seamless integration of the new system with existing clinical trial workflows, managing diverse stakeholder expectations, and maintaining data quality throughout the study. They must also handle tight timelines and adapt quickly to regulatory changes or sponsor requirements. Effective communication with both technical teams and clinical staff is crucial to overcoming these obstacles and ensuring successful project delivery.

What are the key skills and qualifications needed to thrive as an EDC project manager, and why are they important?

To thrive as an EDC Project Manager, you need expertise in clinical data management, project coordination, and a solid understanding of Electronic Data Capture (EDC) systems, usually supported by a degree in life sciences or related fields. Familiarity with EDC platforms like Medidata Rave or Oracle InForm, along with certifications such as PMP or CDISC, is highly valuable. Strong organizational, problem-solving, and communication skills help you effectively lead cross-functional teams and manage client expectations. These competencies ensure successful EDC project delivery, regulatory compliance, and high-quality clinical trial data.

What is an EDC project manager?

EDC Project Managers are professionals who oversee the planning, execution, and monitoring of projects related to Electronic Data Capture (EDC) systems, primarily within clinical research and pharmaceutical industries. They coordinate between cross-functional teams, manage timelines, ensure regulatory compliance, and address any issues that arise during the data collection process. Their goal is to ensure that EDC systems are implemented efficiently and effectively, supporting the overall success of clinical trials. EDC Project Managers also act as the main point of contact for sponsors and stakeholders, ensuring that project objectives and quality standards are met.

What is the difference between Edc Project Manager vs Electrical Project Manager?

AspectEdc Project ManagerElectrical Project Manager
CertificationsPMP, OSHA, EDC-specific trainingPMP, OSHA, Electrical licenses
Work EnvironmentEnergy, utility, and infrastructure projectsConstruction, industrial, and commercial electrical projects
Industry UsageCommon in energy distribution and utility sectorsCommon in construction and industrial sectors
Job FocusDistribution systems, substations, and energy deliveryBuilding wiring, electrical systems, and installations

The Edc Project Manager primarily oversees energy distribution and utility infrastructure projects, focusing on energy delivery systems. In contrast, the Electrical Project Manager handles a broader range of electrical construction projects, including commercial and industrial wiring. Both roles require similar certifications but differ in industry focus and project types.

What are popular job titles related to Edc Project Manager jobs in Cambridge, MA?

For Edc Project Manager jobs in Cambridge, MA, the most frequently searched job titles are:

What job categories do people searching Edc Project Manager jobs in Cambridge, MA look for?

The top searched job categories for Edc Project Manager jobs in Cambridge, MA are:

What cities near Cambridge, MA are hiring for Edc Project Manager jobs?

Cities near Cambridge, MA with the most Edc Project Manager job openings:

Edc Project Manager jobs near you

Director, Clinical Data Management

Alnylam Pharmaceuticals

Cambridge, MA • On-site, Remote

$197K - $266K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago

Job description

Summary
The Director, Clinical Data Management is responsible for the oversight of data management activities in support of Alnylam studies across all stages of clinical drug development. This position reports to the head of the Clinical Data & Insights group.
Responsibilities:
  • Direct and grow internal data management expertise area, including management of direct reports;
  • Direct and establish standards for data management CRO outsourcing strategy and deliverables, including the CRO selection process and the governance of CRO performance;
  • Oversee the successful execution of all data management activities in support of Alnylam clinical studies in partnership with CROs, including eCRF development, database build, data collection, data coding, cleaning, database lock and archiving;
  • Supervise the execution of cross-functional, internal data review plans by direct reports across all Alnylam clinical studies;
  • Partner with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Clinical Pharmacology and Pharmacometrics, Bioanalytical, Safety & Risk Management (SRM) and Regulatory Affairs; CROs, central and local laboratories, and other vendors;
  • Lead development and implementation of data collection standards, consistent with industry best practice;
  • Lead data management contributions to the development of clinical protocols, clinical study reports and other regulatory documents, e.g. DSURs, Briefing Documents, etc.
  • Oversee development of department workflows, and infrastructure strategy and implementation, such as preferred provider initiatives, SOPs, and templates;
  • Collaborate with Statistical Programming and external vendors to ensure compliance of SDTM clinical datasets, consistent with CDISC standards;
  • Collaborate with Clinical Operations and Quality Assurance to certify the integrity and traceability of all clinical data sources, compliant with 21 CFR Part 11 standards;
  • Direct Data Management GCP inspection readiness efforts; function as a leader for Data Management in GCP inspections;
  • Represent Data Management at internal cross-functional meetings and external vendor leadership meetings;
  • Demonstrate clear alignment with Alnylam Core Values including, Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture and Passion for Excellence.

Requirements
  • BS/BA in scientific discipline, MS or equivalent preferred, with at least 15 years of clinical data management experience in a pharmaceutical/biologics/biotechnology company, with at least 5 years in a leadership capacity;
  • Extensive experience managing global studies utilizing an outsourced CDM model from start-up through close-out;
  • Extensive experience managing direct reports and providing performance reviews and career development guidance;
  • Understanding of ICH GCP as well as general knowledge of industry practices and standards;
  • Knowledge and understanding of regulatory requirements and expectations for clinical data systems including 21 CFR Part 11;
  • Expert knowledge of eClinical processes, efficient design/build of an EDC data management system and other Clinical Trial data/Data Management Systems;
  • Expert knowledge and understanding of regulations and industry-adopted data standards, such as CDISC-SDTM and CDASH;
  • Experience using standardized medical terminology, including MedDRA and WHODrug;
  • Experience working with Medidata Rave EDC systems;
  • Experience working with elluminate or other data visualization systems a plus
  • Experience working with MS Office Suite (Excel, Word and PowerPoint) familiar with MS Project;
  • Excellent written and oral communication skills;
  • Highly motivated and flexible, with excellent organizational skills;
  • Ability to work independently and as part of a multi-disciplinary team.

#LI-AB1 #LI-Virtual
U.S. Pay Range
$197,200.00 - $266,800.00
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
About Alnylam
We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

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