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Study Manager Jobs in Harrison, NJ (NOW HIRING)

DM Clinical

Registered Nurse (4122)

Brooklyn, NY · On-site

$65K - $85K/yr

Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood. KNOWLEDGE & EXPERIENCE Education:

MSD

Senior Scientist, Clinical Research

Rahway, NJ · On-site

Ensures appropriate clinical safety assessment and risk management of compounds. Conducts real-time oversight of ongoing trials to identify and mitigate patient, study design, data or study conduct ...

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Study Manager information

See Harrison, NJ salary details

$25.7K

$62.3K

$121.5K

How much do study manager jobs pay per year?

As of Sep 1, 2026, the average yearly pay for study manager in Harrison, NJ is $62,345.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $71,700.00 per year, depending on experience, location, and employer.

What does a study manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.

What are the key skills and qualifications needed to thrive as a study manager?

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

How does a study manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

What is the role of a study manager?

A study manager oversees the planning, execution, and completion of clinical or research studies, ensuring they adhere to protocols, timelines, and regulatory requirements. They coordinate with teams, manage budgets, and monitor progress using tools like project management software to ensure study objectives are met efficiently.

What cities near Harrison, NJ are hiring for Study Manager jobs?

Cities near Harrison, NJ with the most Study Manager job openings:

Study Manager jobs near you
Infographic showing various Study Manager job openings in Harrison, NJ as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 13% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $62,345 per year, or $30 per hour.

Registered Nurse (4122)

DM Clinical

Brooklyn, NY • On-site

$65K - $85K/yr

Other

Posted 18 days ago

Job description

DM Clinical Research is looking to hire an Pharmacy Technician to join our team and work as a Unblinded CRC to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.
Duties & Responsibilities:
  • Compound and dispense prescribed IP as needed by Sponsor approved protocol
  • Measure vital signs (blood pressure, pulse, temperature, weight) and document medical histories.
  • Collect blood (phlebotomy), urine, and other specimens for testing.
  • Administer injections or vaccines, and monitor patients for adverse reactions.
  • Provide consultative support regarding the preparation and dosing of drugs
  • Run routine tests like EKGs (electrocardiograms).
  • Supervise and maintain records of all medications
  • Perform regular audits on the clinical data to assess percent completeness and accuracy
  • Ensure external sites' regulatory documents and required site certifications are up to date
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction
  • Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting
  • Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.

KNOWLEDGE & EXPERIENCE
Education:
  • Associates Degree required or 2 years of formal educational coursework
  • Bachelor's degree, preferred
  • Secondary or Foreign Medical Graduate, preferred

Experience:
  • 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
  • 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
  • 1+ year utilizing CRIO, preferred

Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
  • Pharmacy Technician Certification, preferred
  • Completion of DMCR-required training, including GCP, OSHA and IATA

Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
  • Excellent communication and customer service skills, both written and verbal
  • Excellent time-management skills
  • Bilingual (Spanish) preferred

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