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Edc Project Manager Jobs in New Jersey (NOW HIRING)

Winaxis

Clinical Research Coordinator

Jersey City, NJ · On-site

$25.25 - $33.75/hr

... EDC) Trial Master File (TMF) Regulatory Documentation Adverse Event Reporting Data Management ... projects How to Apply Interested candidates can submit their updated resume along with a cover ...

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Edc Project Manager information

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 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 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.

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 platforms. Candidates should verify specific job postings for remote work availability.

What are popular job titles related to Edc Project Manager jobs in New Jersey?

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

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

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

What cities in New Jersey are hiring for Edc Project Manager jobs?

Cities in New Jersey with the most Edc Project Manager job openings:

Edc Project Manager jobs near you
Infographic showing various Edc Project Manager job openings in New Jersey as of August 2026, with employment types broken down into 83% Full Time, 15% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution.

Senior Clinical Data Manager

Everest Clinical Research

Bridgewater, NJ • On-site, Remote

$90K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago

Job description

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's Corporate headquarters are located in Ontario, Canada and US headquarters in New Jersey, USA, with additional physical offices in Asia and Europe.
Everest is known in the industry for its high-quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us...that's Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Clinical Data Managers for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Key Accountabilities:
Lead Data Management Activities, Perform Training and Client Relationship Management
  1. Develop and maintain Data Management Project Plan (Plan). Document deviations from the Plan, log and report issues, and follow up on their resolutions.
  2. Is the primary contact person for day to day data management activities, and is the person ultimately responsible for all data management deliverables for assigned projects.
  3. Is the primary contact person for communication and discussion of topics related to data management timelines and deliverables; request for out of scope tasks; first line contact for technical or procedural issues.
  4. Is responsible for planning and implementing data management timelines and deliverables; and is responsible for providing database and data management activities status reports; contributes to the overall project planning, progress tracking and reporting.
  5. Assist with study-level resource planning and management, including the review of team members' timesheet reports.
  6. Assist in performing client relationship management activities. Participate in project bid defense meeting when required.
  7. Perform training on electronic data capture (EDC) system, dataflow and quality control processes to clinical trial personnel.
  8. Provide training to new data management personnel on data management processes and procedures. Perform QC review of work performed by less experienced data management personnel.
  9. Assist in generation of project Work Orders and Amendments.
  10. Assist in management of dataflow from and performance of Third Party Vendors (Non-CRF data vendors).
  11. Participate in project kick off meeting, investigators meeting, and regular project management team meeting.
  12. Provide support to client audits and regulatory inspections. Follow up on audit findings.
  13. Create and maintain clinical trial Data Management Study Binders.

Perform Hands-on Data Management Activities
  1. Design and review case report forms (CRFs/eCRFs). Develop and review Case Report Form Completion Instructions. Generate and review annotated Case Report Forms.
  2. Design and review Clinical Trial Source Document templates and completion instructions when required.
  3. Develop and maintain data validation specifications.
  4. Develop and maintain Data Management Plan (DMP). Document deviations from the DMP.
  5. Participate in the database design process. Participate in EDC User Acceptance Testing (UAT).
  6. Manage the process of database modifications (after go-live) due to protocol amendments or study needs.
  7. Develop and maintain Data Quality Review Plan (DQRP). Coordinate with programmers to complete the programming and validation of the listings and summary tables as specified in the DQRP.
  8. Perform Third Party non-CRF data management activities.
  9. Review data, issue and resolve queries. Assist Investigative Site personnel with resolving queries.
  10. Perform Serious Adverse Event reconciliation.
  11. Assist in resolving medical coding discrepancies resulting from coding of medical history, adverse events, procedures and medicinal products.
  12. Cooperate and assist the Quality Assurance Department with quality control audits on assigned databases.
  13. Perform database soft-lock and hard lock activities.
  14. Maintain and prepare final archival of data management documentation relevant to the assigned clinical trials, and assist the corporate archivist in assembling and archiving such documentation.

Qualifications and Experience:
  1. A Bachelors' or Master's degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields.
  2. At least 5 years of experience in pharmaceutical clinical trial data management or at least 2 year of experience as a Clinical Data Manager II, with demonstrated knowledge, experience and ability to perform to meet high quality standards and high level of customer satisfaction.
  3. Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards
  4. Demonstrated a strong leadership in clinical data management activities and a desire to excel in leading data management projects.

Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a 401(k) retirement / pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $90,000 - $130,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
#LI-Remote
#LI-KD1
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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