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Edc Project Manager Jobs in Pennsylvania (NOW HIRING)

Ocugen Inc

Senior Clinical Data Manager

Malvern, PA · On-site

Take the lead on special projects and additional tasks as required by management. * Lead the ... Experience with CRFs, and in the development process of EDC databases, IRT systems and diary ...

Alpha Life Sciences

$120 - $180/hr

... EDC and Data Management, and Agile Trial Management. About the Role AlphaLife Sciences is looking for a Medical Writer Project Director to lead and coordinate our network of external medical writing ...

Novocure

Clinical Trial Lead

Wayne, PA · Hybrid

$147K - $190K/yr

Experience managing CROs, vendors, study budgets, and project timelines. * Strong knowledge of ICH ... Experience with CTMS, eTMF, and EDC systems. * Advanced degree (MS, PharmD, or PhD). HOW YOU'LL ...

Novocure

Clinical Trial Lead

Philadelphia, PA · Hybrid

$147K - $190K/yr

Experience managing CROs, vendors, study budgets, and project timelines. * Strong knowledge of ICH ... Experience with CTMS, eTMF, and EDC systems. * Advanced degree (MS, PharmD, or PhD). HOW YOU'LL ...

Novocure

Clinical Trial Lead

Wayne, PA · On-site

$147K - $190K/yr

Experience managing CROs, vendors, study budgets, and project timelines. * Strong knowledge of ICH ... Experience with CTMS, eTMF, and EDC systems. * Advanced degree (MS, PharmD, or PhD). HOW YOU'LL ...

Doist

eCOA Senior Technical Consultant

Conshohocken, PA · On-site

$90 - $130/hr

Collaborate with Project Managers, Customer Care, Product, Development, Quality, and Integration ... Experience with eCOA, IRT, EDC, SaaS, or clinical trial technology. * Experience working with ...

Actalent

Registered Nurse (Research)

Philadelphia, PA · On-site

$40 - $45/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Enter study data into electronic data capture (EDC) systems and other databases with a high level ... Collaborate closely with study physicians, research coordinators, project managers, and other ...

ZS

Clinical Data Manager

Philadelphia, PA · On-site

ZS is seeking a Tech Project Delivery Manager to lead a high-velocity team focused on the future of ... EDC, ePRO, Labs, CDMS * Biometrics Platforms: Hands-on experience delivering CDR and/or SCE ...

CSL

Senior Clinical Scientist

King Of Prussia, PA · On-site

With a streamlined, project-led structure and a focus on collaboration, we're building a future ... Manage the processes and partnerships required to support external study oversight committees (e.g.

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All JobsEdc Project JobsEdc Project Manager JobsEdc Project Manager Jobs in Pennsylvania

Edc Project Manager information

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 Pennsylvania?

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

What job categories do people searching Edc Project Manager jobs in Pennsylvania look for?

The top searched job categories for Edc Project Manager jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Edc Project Manager jobs?

Cities in Pennsylvania with the most Edc Project Manager job openings:

Edc Project Manager jobs near you
Infographic showing various Edc Project Manager job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, 1% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

Senior Clinical Data Manager

Ocugen Inc

Malvern, PA • On-site

Other

Posted 11 days ago

Job description

Position Summary
The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data collection and management processes, and contribute to critical aspects of clinical trial data handling, including database design, CRF development, data monitoring, and validation for clinical development programs and marketed products. In addition to technical responsibilities, the Senior Clinical Data Manager will provide leadership to junior data management staff and work collaboratively across functional teams, ensuring high-quality and timely deliverables.
Responsibilities
  • Oversee studies or a program, ensures cross study consistency, mentors team members, and manage vendors as needed.
  • Makes higher level decisions on data standards, risk based data management strategies, and protocol driven design choices.
  • Leads inspection readiness, ensures documentation completeness across studies,
  • Serves as a subject matter expert during audits, helps standardize SOP alignment, guides the team in applying GCP, ICH, CDISC, and internal compliance expectations.
  • Provides strategic input to Clinical Operations, Biostatistics, Programming, and Quality on data flow, database design improvements, standards adoption, and process optimizations.
  • Represents DM in program level meetings and drives improvements across studies (aligned with broader responsibilities seen in senior and principal level descriptions).
  • Provide mentorship and technical guidance to junior data management staff.
  • Ensure accurate and efficient collection of electronic clinical trial data.
  • Develop and validate edit checks and validation reports to maintain the highest quality data.
  • Ensure all required documentation is completed accurately and promptly across studies.
  • Develop and implement innovative data strategies to streamline data management workflows.
  • Identify and mitigate risks in data management processes proactively.
  • Take the lead on special projects and additional tasks as required by management.
  • Lead the development and execution of data management plans (DMPs), ensuring seamless data flow from collection to final analysis.
  • Design and oversee program standards and study-specific electronic Case Report Forms (eCRFs).
  • Partner with Biometrics, Clinical, and Regulatory teams to implement research protocols and ensure proper clinical data outputs for deliverables.
  • Develop and manage data transfer specifications, data review plans, and risk management strategies.
  • Collaborate on cross-functional project timelines and ensure database deliverables are achieved within schedule and quality standards.
  • Author and revise standard operating procedures (SOPs) and study-specific DMPs.
  • Prepare for and participate in audits, ensuring data management processes meet compliance standards.

  • BS degree in clinical, biological or mathematical sciences, or related field, or nursing qualification, or work- related equivalent.
  • 5-7 years of clinical data management experience in biopharma or CRO environment.
  • Strong attention to detail and motivation to provide quality deliverables.
  • Able to work in a fast-paced environment.
  • Experience with clinical trials.
  • Experience with CRFs, and in the development process of EDC databases, IRT systems and diary applications for data collection. Veeva experience is preferred.
  • Strong knowledge of GCPs, ICH, FDA, and CDISC regulatory requirements governing clinical studies.
  • Demonstrated attention to detail and outstanding organization skills.
  • Self-motivated with a commitment to high quality, on-time deliverables.
  • Excellent communication and collaboration skills with a team-oriented approach.
  • Demonstrated ability to identify and resolve issues and effectively manage timelines.

Working Conditions
This position operates in an office setting, in person. Remote work will be limited. Job may additionally require incumbent to be available outside of these hours to handle priority business needs.
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About Ocugen

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

Malvern, PA, US

Year founded

2013

Social media

Twitter

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