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Clinical Site Manager Jobs in Riverside, NJ (NOW HIRING)

DM Clinical

Site Manager (3768)

Philadelphia, PA · On-site

$100K - $120K/yr

The Site Manager's job is to ensure that quality research is conducted at assigned investigative ... Ensuring clinical trial management from FPFV to study close out with strict adherence to study ...

JERSEY COLLEGE

Nursing Clinical Coordinator

Ewing, NJ · On-site

The Nursing College Clinical Site Liaison is responsible for managing the practicum experiences (both direct supervision and preceptorships) for our Practical Nurse and Registered Nurse programs. The ...

Jersey College

Nursing Clinical Coordinator

Ewing, NJ · On-site

$90K/yr

The Nursing College Clinical Site Liaison is responsible for managing the practicum experiences (both direct supervision and preceptorships) for our Practical Nurse and Registered Nurse programs. The ...

ICON

Site Contract Manager

Blue Bell, PA · On-site +1

Site Contract Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Icon plc

Site Contract Manager

Blue Bell, PA

Site Contract Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Myoderm

Manager, Direct to Site (US)

PA · On-site

... and managing the Direct to Site (DTS) team in the US to support the needs of any project that ... Work closely with clients to determine clinical trial requirements and develop appropriate supply ...

Myoderm

Manager, Direct to Site (US)

Norristown, PA

... and managing the Direct to Site (DTS) team in the US to support the needs of any project that ... Work closely with clients to determine clinical trial requirements and develop appropriate supply ...

Icon plc

Site Contracts Lead

Blue Bell, PA · On-site +1

$85K - $113K/yr

Managing end-to-end site contracting activities for assigned studies, including template use ... Strong experience in clinical site contracting or similar contract negotiation roles within CRO ...

Hassman Research Institute

Patient Liaison

Evesham, NJ · On-site

Communicates on a regular basis with clinical site management * Follows Good Clinical Practice guidelines and OSHA regulations and guidelines Additional Information All your information will be kept ...

MSD

Senior Scientist, Clinical Research

West Point, PA · On-site

The Early Clinical Scientist (ECS) coordinates the design, planning and execution of early phase ... g. site monitoring plan, study operations manual, informed consent, etc.). Project Management ...

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Showing results 1-20

All JobsClinical Site JobsClinical Site Manager JobsClinical Site Manager Jobs in Riverside, NJ

Clinical Site Manager information

See Riverside, NJ salary details

$25.3K

$80.8K

$122.7K

How much do clinical site manager jobs pay per year?

As of Jul 14, 2026, the average yearly pay for clinical site manager in Riverside, NJ is $80,813.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,500.00 and $122,200.00 per year, depending on experience, location, and employer.

What are some common challenges Clinical Site Managers face when overseeing multiple clinical trial sites, and how can they effectively address them?

Clinical Site Managers often juggle responsibilities across several trial sites, which can lead to challenges such as maintaining consistent protocol compliance, ensuring timely patient recruitment, and managing communication among diverse teams. To address these issues, successful Site Managers prioritize clear communication, establish regular check-ins with site staff, and utilize robust project management tools to track progress and resolve issues quickly. Building strong relationships with site personnel and proactively identifying bottlenecks also helps ensure the trials run smoothly and on schedule.

What are the key skills and qualifications needed to thrive as a Clinical Site Manager, and why are they important?

To thrive as a Clinical Site Manager, you need a deep understanding of clinical research protocols, regulatory compliance, and project management, usually supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are typically required. Strong leadership, organizational skills, and effective communication set exceptional Clinical Site Managers apart. These competencies are essential for ensuring clinical trials are conducted efficiently, ethically, and in accordance with regulatory standards.

What does a Clinical Site Manager do?

A Clinical Site Manager is responsible for overseeing the daily operations of clinical trial sites. Their main duties include managing staff, ensuring study protocols are followed, maintaining compliance with regulatory requirements, and serving as a liaison between sponsors, investigators, and site personnel. They are also tasked with monitoring patient recruitment, ensuring data quality, and resolving any issues that arise during the trial. Ultimately, they help ensure that clinical trials are conducted efficiently, safely, and in accordance with all guidelines.

What is the difference between Clinical Site Manager vs Clinical Research Coordinator?

AspectClinical Site ManagerClinical Research Coordinator
CredentialsBachelor's degree, experience in clinical trials, sometimes certificationBachelor's degree, often certification in clinical research
Work EnvironmentOversees entire site operations, manages staff, ensures complianceAssists with participant recruitment, data collection, and study procedures
Employer & IndustryResearch institutions, pharmaceutical companies, CROsResearch sites, hospitals, clinics, academic institutions

The Clinical Site Manager and Clinical Research Coordinator roles both operate within clinical research environments. The Site Manager oversees site operations and staff, while the Coordinator handles participant interactions and data collection. Both roles require related credentials and are essential for successful clinical trials, but they differ in scope and responsibilities.

What cities near Riverside, NJ are hiring for Clinical Site Manager jobs? Cities near Riverside, NJ with the most Clinical Site Manager job openings:
Clinical Site Manager jobs near you
Infographic showing various Clinical Site Manager job openings in Riverside, NJ as of July 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 62% In-person, and 38% Remote job distribution, with an average salary of $80,813 per year, or $38.9 per hour.

Site Manager (3768)

DM Clinical

Philadelphia, PA • On-site

$100K - $120K/yr

Other

Posted 26 days ago

Job description

The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Also To ensure study enrollment meets or exceeds Sponsors' expectations and company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
  • Responsible for immediate supervision and performance of the assigned site staff under the supervision of the Site Director or Director of Site Operations.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
  • Sponsor-provided and IRB-approved Protocol Training
  • All relevant Protocol Amendments Training
  • Any study-specific Manuals Training as applicable
  • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • It is the responsibility of the Site Manager to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
  • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow-up on the action items, at their respective sites.
  • Make sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study-related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
  • Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs, and guidance documents.
  • Ensuring data quality, subject retention, and compliance, timely and adequate study data reporting on the assigned protocol(s) being conducted at their respective site(s).
  • Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
  • Coaching, counseling, and disciplining the employees as applicable.
  • To develop, coordinate, and enforce site-specific systems, policies, procedures, and productivity standards.
  • Communicating and effective implementation of strategic goals from senior management to the site team.
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
  • Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
  • Facilitate effective communication between patients, healthcare providers, and research staff
  • Any other matters as assigned by management.

KNOWLEDGE & EXPERIENCE
Education:
  • Bachelor's degree preferred
  • Advanced degree preferred

Experience:
  • At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization.

Credentials:
  • Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.

Knowledge and Skills:
  • Solid teamwork, organizational, interpersonal, and problem-solving skills and attention to detail.
  • Critical Thinking
  • Active Listening
  • Reading Comprehension - Understanding written sentences and paragraphs in work-related documents.
  • Speaking and Writing to communicate effectively as appropriate for the needs of the audience.
  • Ability to multitask, adhere to deadlines, and work both independently and cooperatively with interdisciplinary teams.
  • Strong computer skills in relevant software and related clinical systems are required.
  • Comprehensive knowledge of FDA regulations, ICH-Good Clinical Practices (GCP) and ISOs.
  • Proficient communication and comprehension skills both verbal and written in the English language are required.
  • Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.

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