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Study Start Up Associate Jobs in Union, NJ (NOW HIRING)

Winaxis

Clinical Research Coordinator

Jersey City, NJ · On-site

$25.25 - $33.75/hr

Ensure protocol compliance and participant safety throughout the study. Assist with study start-up, close-out activities, and regulatory submissions. Required Qualifications Bachelor's or Master ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Provide medical oversight for assigned clinical studies from study start-up through closeout. * Participate in protocol development, protocol amendments, informed consent review, and clinical study ...

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Showing results 41-60

All JobsStudy Start Up Associate JobsStudy Start Up Associate Jobs in Union, NJ

Study Start Up Associate information

See Union, NJ salary details

$12

$32

$56

How much do study start up associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for study start up associate in Union, NJ is $32.14, according to ZipRecruiter salary data. Most workers in this role earn between $21.54 and $42.36 per hour, depending on experience, location, and employer.

What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?

AspectStudy Start Up AssociateClinical Trial Coordinator
Required CredentialsBachelor's degree, knowledge of regulatory requirementsBachelor's degree, familiarity with clinical procedures
Work EnvironmentRegulatory and site initiation activitiesParticipant management and site coordination
Employer & Industry UsagePharmaceuticals, biotech, CROsHospitals, research centers, CROs

The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.

What are popular job titles related to Study Start Up Associate jobs in Union, NJ?

For Study Start Up Associate jobs in Union, NJ, the most frequently searched job titles are:

What job categories do people searching Study Start Up Associate jobs in Union, NJ look for?

The top searched job categories for Study Start Up Associate jobs in Union, NJ are:

What cities near Union, NJ are hiring for Study Start Up Associate jobs?

Cities near Union, NJ with the most Study Start Up Associate job openings:

Study Start Up Associate jobs near you
Infographic showing various Study Start Up Associate job openings in Union, NJ as of June 2026, with employment types broken down into 1% As Needed, 38% Full Time, 48% Part Time, 1% Temporary, 11% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $66,852 per year, or $32.1 per hour.

Clinical Research Coordinator

Winaxis

Jersey City, NJ • On-site

$25.25 - $33.75/hr

Full-time

Medical, PTO

Posted 5 days ago

Job description

Job Title : Clinical Research Coordinator (CRC) Experience : 0–3 Years Location : Dallas, Texas Employment Type : Full-time Job Summary:- We are looking for a motivated and detail-oriented Clinical Research Coordinator to support the planning, execution, and management of clinical research studies. The ideal candidate should have 0–3 years of experience in clinical research and a strong understanding of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Fresh graduates with relevant internships or clinical research training are encouraged to apply. Key Responsibilities Coordinate and manage clinical research studies in compliance with study protocols, ICH-GCP guidelines, and applicable regulations. Screen, recruit, and enroll study participants. Obtain informed consent from study participants. Schedule and coordinate patient visits and follow-up appointments. Collect, verify, and maintain accurate study documentation and source data. Enter clinical data into Electronic Data Capture (EDC) systems. Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents. Report adverse events and serious adverse events according to protocol and regulatory requirements. Coordinate with investigators, sponsors, CROs, and ethics committees. Prepare for monitoring visits, audits, and regulatory inspections. Ensure protocol compliance and participant safety throughout the study. Assist with study start-up, close-out activities, and regulatory submissions. Required Qualifications Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field. 0–3 years of experience in clinical research or clinical trial coordination. Knowledge of ICH-GCP, FDA, and local regulatory guidelines. Familiarity with EDC systems and Microsoft Office. Strong organizational, communication, and documentation skills. Ability to work independently and as part of a multidisciplinary team. Preferred Qualifications GCP Certification. Clinical Research certification is an added advantage. Experience with site coordination or patient recruitment. Knowledge of clinical trial documentation and regulatory submissions. Key Skills Clinical Trial Coordination ICH-GCP Compliance Patient Recruitment Informed Consent Process Source Documentation Electronic Data Capture (EDC) Trial Master File (TMF) Regulatory Documentation Adverse Event Reporting Data Management Communication & Coordination Attention to Detail Time Management Benefits Competitive salary Health insurance Performance-based incentives Training and career development opportunities Paid leave and holidays Exposure to global clinical research projects How to Apply Interested candidates can submit their updated resume along with a cover letter highlighting their clinical research experience, certifications, and relevant skills.