ZipRecruiter

Log In

1

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

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 ...

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 ...

Stago

Lab Technologist

Mount Olive, NJ · On-site

$70K - $85K/yr

Verify technical conditions prior to the start of a study, ensure instruments are in pristine working order and maintenance of equipment is up to date to ensure successful study conditions.

previous page

Showing results 41-60

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

Study Start Up Associate information

See Edison, NJ salary details

$13

$32

$57

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 Edison, NJ is $32.65, according to ZipRecruiter salary data. Most workers in this role earn between $21.92 and $43.03 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 Edison, NJ?

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

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

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

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

Cities near Edison, 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 Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 15% Part Time, and 15% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $67,916 per year, or $32.7 per hour.

Director Medical Monitor

System One

Parsippany, NJ • On-site

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 22 days ago

Job description

Job Title: Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid – onsite Overview Responsibilities

  • 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 report preparation.
  • Serve as the primary medical contact for investigators and study sites regarding protocol-related medical questions, including subject eligibility and enrollment guidance.
  • Conduct ongoing medical review of subject safety data, eligibility determinations, protocol deviations, and emerging risk signals to ensure patient safety and scientific integrity.
  • Review and interpret clinical data and trends, including safety data, laboratory values, adverse events, and protocol deviations.
  • Support dose escalation decisions and safety review meetings, where applicable.
  • Provide medical training and support site initiation visits, investigator meetings, monitoring activities, and data review committees (e.g. DSMB) as needed.
  • Collaborate with Pharmacovigilance teams on safety reporting requirements, safety management plans and risk mitigation strategies, and escalate safety concerns when needed.
  • Collaborate with Clinical Operations to ensure studies are conducted timely and in compliance with GCP, SOPs, and regulatory guidelines.
  • Support Regulatory Affairs in regulatory submissions and responses to regulatory agencies.
  • Contribute to audit and inspection readiness activities.
Requirements
  • MD or DO required; Board eligible/certified preferred.
  • Infectious Diseases expertise preferred.
  • 5-8 years clinical drug development experience.
  • Experience in the design, conduct and analysis of Phase 1-4 studies; experience in global clinical trials and with CROs preferred.
  • Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory requirements.
  • Strong analytical and problem-solving abilities with the ability to interpret clinical and safety data and apply sound medical judgment.
  • Excellent communication and presentation skills.
  • Leadership and cross-functional collaboration skills in a fast-paced environment.
  • Experience reviewing clinical and safety data listings, narratives, and aggregate analyses.
  • Additional clinical research training or certification or regulatory experience is a plus.
  • Willingness to travel up to 25% for investigator meetings, site visits, and clinical study activities as needed.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #568-Clinical

System One logo

About System One

Sourced by ZipRecruiter

System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US

View All System One Jobs