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Clinical Project Associate Jobs in Madison, NJ (NOW HIRING)

Clinical Project Lead

East Brunswick, NJ ยท On-site

$92 - $120/hr

The Clinical Project & Quality Improvement Lead is responsible for managing a variety of clinical ... As a Certified Medical Assistant/Patient Care Associate, you will be responsible for providing ...

The Clinical Project & Quality Improvement Lead is responsible for managing a variety of clinical ... As a Certified Medical Assistant/Patient Care Associate, you will be responsible for providing ...

Project Associate - Epic

Secaucus, NJ ยท On-site

$66K - $93K/yr

The Project Associate is a key member of the Epic Transformation team, organizing program/workgroup ... Liaise with various teams, including IT, security, and clinical departments, to ensure seamless ...

To lead the process of clinical project feasibility during standalone feasibility (awarded ... Collecting data from data assets as well as country associates, site level Investigators, and KOL ...

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Clinical Project Associate information

See Madison, NJ salary details

$13

$32

$56

How much do clinical project associate jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for clinical project associate in Madison, NJ is $32.51, according to ZipRecruiter salary data. Most workers in this role earn between $21.83 and $42.88 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a clinical project associate?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

What is the difference between Clinical Project Associate vs Clinical Research Coordinator?

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What cities near Madison, NJ are hiring for Clinical Project Associate jobs?

Cities near Madison, NJ with the most Clinical Project Associate job openings:

Infographic showing various Clinical Project Associate job openings in Madison, NJ as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $67,623 per year, or $32.5 per hour.

Clinical Project Lead

Astera Cancer Care

East Brunswick, NJ โ€ข On-site

$92 - $120/hr

Other

Posted 5 days ago


Job description

Why Join Us?For us, what matters most is excellence. We are caring professionals, people who live, work and dedicate themselves to the communities within New Jersey and Pennsylvania. As such, we strive to provide a sanctuary of excellence, precision, thoroughness and genuine compassion. We also take a whole-person approach to patient care and treatment, tailoring all that we do around their unique needs. And we do all we can for patients, going the extra mile to see that theyโ€™re supported, informed and getting the one-on-one care and service they deserve.Job Description:JOB SUMMARY:The Clinical Project & Quality Improvement Lead is responsible for managing a variety of clinical projects, quality improvement initiatives, and safety programs across departments. Acting as a critical thinker who makes sound decisions independently, this role provides structured leadership and oversight to optimize front-line clinical operations, improve workflow processes, ensure regulatory compliance, and elevate patient care and safety.ESSENTIAL FUNCTIONS:Project Leadership & Implementation: Acts as a lead for clinical project and quality initiative teams, driving the design, development, execution, and implementation phases of multiple sustainable outcome improvement projects simultaneously.Team Facilitation & Coaching: Establishes team membership, motivates members, facilitates meetings, and provides hands-on coaching, mentoring, and direction to diverse project teams and unit councils.Strategic Planning & Mapping: Develops comprehensive project plans that identify key issues, approaches, resource requirements, key driver diagrams, and performance metrics using process/system mapping and reliability science strategies.Workflow & Process Optimization: Collaborates across departments with leadership and initiative-focused groups to identify opportunities to improve workflow processes, deliver successful results, and build a strong culture of quality and safety.Data-Driven Evaluation: Reviews, analyzes, and trends performance data against internal and external benchmarks; creates run charts, PDSA testing documentation, and timely progress reports to drive scorecard improvements.Regulatory Compliance: Identifies improvement priorities based on evidence-based practice while ensuring strict compliance with internal standards and external regulatory/accrediting agencies (e.g., The Joint Commission, OSHA, Department of Health, and Federal/State codes).Risk & Event Management: Analyzes and investigates clinical event reports, brings concerns to local safety huddles, encourages transparent reporting, and ensures appropriate referral, escalation, and follow-up (including RCA-2 processes as needed).Stakeholder Liaison & Communication: Acts as the primary point of contact, liaison, and problem solver for project teams; provides timely, actionable feedback and reports to clinical, administrative, and support staff across all levels of the organization.Workforce & Knowledge Dissemination: Assesses project impacts on the workforce, collaborates on training programs for various audiences, and advances clinical science by sharing project outcomes, lessons learned, and best practices internally and at professional forums.KNOWLEDGE, SKILLS & ABILITIES:Strong organizational, analytical, and critical thinking skills are essential.Excellent written and oral communication skills with the ability to present complex data and project outcomes to various levels within the organization.Proficiency in the use of computer applications and software including Outlook, Word, PowerPoint, and Excel.Expert knowledge of clinical operations, patient safety programs, ahd high-reliability science.EDUCATION & EXPERIENCE:Bachelorโ€™s degree in Nursing, Healthcare, or Health Science required (Bachelor of Science in Nursing strongly preferred).Minimum of 5 years of experience in healthcare required, with at least 2 years of dedicated project planning or performance improvement experience.Experience as a clinician in an outpatient ambulatory setting strongly preferred.Experience in statistics or clinical research is a plus.LICENSES & CERTIFICATIONS:CPPS (Certified Professional in Patient Safety), PMP (Project Management Professional), Oncology Nursing, or equivalent professional certification required at the time of hire or within 1โ€“2 years of hire.PHYSICAL REQUIREMENTS:Must be willing and able to travel between Astera/Solara regional sites or facilities as required by project scope.As a Certified Medical Assistant/Patient Care Associate, you will be responsible for providing clinical and administrative support to ensure the efficient operation of our Primary Care office. You will support doctors and patients through a variety of tasks related to patient care management and communicate with accuracy, quality and timeliness. Float to the Old Bridge / Sayreville/East Brunswick/ Edison locations.Duties include: Taking and recording vital signs and EKGs. Preparing patients for examinations. Obtain and update patient medication lists and give injections. Authorizing prescription refills as directed by physicians. EMR, rooming patients, clerical work, if needed.Requirements:Medical Assistant Certification requiredProven working experience as a medical assistant and/or medical secretaryKnowledge of medical office management systems and proceduresExcellent time management skills and ability to multi-task and prioritize workExcellent written and verbal communication skillsStrong organizational and planning skillsPay Range: $92K - $120K annuallyPay Transparency: The above reflects the anticipated pay range for this position. The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills and professional experience. #J-18808-Ljbffr