ZipRecruiter

Log In

1

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

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 ...

previous page

Showing results 41-60

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

Edc Project Manager information

See Boston, MA salary details

$41.8K

$111.6K

$176K

How much do edc project manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for edc project manager in Boston, MA is $111,554.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,300.00 and $133,600.00 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 Boston, MA? For Edc Project Manager jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Edc Project Manager jobs in Boston, MA look for? The top searched job categories for Edc Project Manager jobs in Boston, MA are:
What cities near Boston, MA are hiring for Edc Project Manager jobs? Cities near Boston, MA with the most Edc Project Manager job openings:
Edc Project Manager jobs near you

Site Management Leader (SML)

Tango Therapeutics

Boston, MA • On-site

$128K - $192K/yr

Full-time

Re-posted 3 days ago

Job description

Company Overview
Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.
Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.
This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.
The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts.
Summary
We are seeking a Site Management Leader (SML) to oversee all site management and monitoring activities conducted by the CRO in a clinical trial. This role will be assigned to critical clinical trials of the Tango portfolio and serve as the primary contact between sponsor and CRO for site management aspects.
In a fast-paced, small biotech environment, the SML will operationally oversee and manage the end-to-end site management activities as per approved timelines, budget, regulatory requirements, and internal standards. This individual will play a key role in the execution and delivery of clinical trial objectives.
The ideal candidate is highly collaborative, detail-oriented, and comfortable operating in a hands-on environment, with a focus on building scalable processes, tools, and best practices to support efficient and compliant clinical trial execution.
Your role
  • Serve as the primary liaison between CTT and CRO for all site management activities
  • Oversee CRO performance for site management to ensure compliance with contractual obligations, timelines, and quality standards
  • Lead or contribute to the development of the Site Management Oversight Plan and other trial-specific operational plans in collaboration with CTT
  • Contribute to the development of a site-related RBQM framework to drive efficiency and ensure quality of critical site management aspects
  • Identify trial-level risks and contribute to the development and implementation of risk management and mitigation strategies
  • Manage and monitor site identification, feasibility assessments, and site selection processes
  • Ensure site readiness for initiation, including training, documentation, and logistical preparedness
  • Oversee and support site initiation visits (SIVs) and ensure timely site activation
  • Monitor patient recruitment strategies and enrollment progress across clinical sites
  • Ensure protocol compliance and data integrity through oversight of site monitoring activities
  • Review monitoring visit reports and ensure timely resolution of site issues and follow-up actions
  • Collaborate with CRO to address site-level issues. Escalate unresolved issues to CTL and CTT, as needed
  • Ensure adherence to ICH GCP, regulatory requirements, and internal SOPs throughout trial conduct
  • Participate in audits, inspections, and quality assurance activities related to site management
  • Oversee site closure activities and ensure proper documentation and archiving

What You Bring
  • 5+ years of trial management experience with 3+ years in site management. Leadership experience (preferred)
  • Bachelor's degree in Life Sciences, Pharmacy or related field
  • Experience working in global clinical development organization
  • Experience in Oncology development (preferred)
  • Knowledge of ICH-GCP, FDA guidelines, EU CTR and other relevant guidelines
  • Knowledge of trial/ site risk assessment and management
  • Direct experience with site health authority inspections (FDA, EMA, MHRA, etc.) incl. sponsor GCP inspections (preferred)
  • Experience in outsourcing and oversight
  • 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 the ability to lead cross-functional teams
  • Strong interpersonal and communication skills
  • Strong analytical thinking and decision-making capabilities
  • Willingness to travel, as required (typically 10 - 20%)

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
#LI-Hybrid
Salary range
$128,000-$192,000 USD

Apply