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Clinical Research Doctor Jobs (NOW HIRING)

Frontage Laboratories

Clinical Research Nurse

Secaucus, NJ · On-site

$45 - $55/hr

Clinical Research Nurse (per diem) Title: Clinical Research Nurse (per diem) Location: Secaucus, NJ ... Administer Medications (including IV administration route) per doctor's and protocol instructions.

Frontage Laboratories

Clinical Research Nurse

Secaucus, NJ · On-site

$45 - $55/hr

Clinical Research Nurse (per diem) Title: Clinical Research Nurse (per diem) Location: Secaucus, NJ ... Administer Medications (including IV administration route) per doctor's and protocol instructions.

Envista

Clinical Research Manager

Brea, CA · On-site

$125K - $153K/yr

The Clinical Research Manager is responsible for managing all US clinical usability studies for ... Doctor of Dental Science (DDS) or similar degree plus 5 years of relevant dental experience ...

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How much do clinical research doctor jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical research doctor in the United States is $72.98, according to ZipRecruiter salary data. Most workers in this role earn between $59.13 and $74.76 per hour, depending on experience, location, and employer.

What is a clinical research doctor?

Clinical research doctors are medical professionals who design, conduct, and oversee clinical trials to evaluate new drugs, treatments, or medical devices. They play a critical role in advancing medical knowledge and ensuring that new therapies are safe and effective for patients. These doctors work closely with research teams, regulatory agencies, and patients throughout the research process. Their work helps to bring innovative treatments from the laboratory to clinical practice.

What are the key skills and qualifications needed to thrive as a clinical research doctor, and why are they important?

A Clinical Research Doctor requires a medical degree (MD or equivalent), deep knowledge of clinical trial protocols, and expertise in research methodologies. Familiarity with data analysis software, electronic data capture systems, and regulatory compliance (such as GCP certification) is typically required. Outstanding critical thinking, attention to detail, and strong communication skills help build trust and ensure ethical, accurate study conduct. These competencies are crucial for ensuring the integrity, safety, and effectiveness of clinical research, ultimately advancing patient care.

What are some typical challenges a clinical research doctor faces when overseeing clinical trials?

Clinical Research Doctors often encounter challenges such as ensuring patient recruitment meets study requirements, maintaining strict adherence to regulatory guidelines, and managing unexpected adverse events. Coordinating with multidisciplinary teams, including research coordinators, nurses, and data managers, is essential to keep trials running smoothly. Additionally, balancing clinical responsibilities with research obligations can require strong organizational and time-management skills. Addressing these challenges effectively helps ensure the integrity and success of clinical trials.

What is the difference between Clinical Research Doctor vs Clinical Research Coordinator?

AspectClinical Research DoctorClinical Research Coordinator
Required CredentialsMedical degree (MD), clinical research trainingBachelor's degree, research training often preferred
Work EnvironmentHospitals, research institutions, clinical trial sitesResearch sites, hospitals, clinics
Employer & Industry UsageAcademic medical centers, pharmaceutical companiesResearch organizations, hospitals, CROs
Common Search & ComparisonOften compared for clinical trial oversight rolesCompared for research coordination and management roles

The Clinical Research Doctor typically holds a medical degree and oversees clinical trials, ensuring patient safety and protocol compliance. In contrast, the Clinical Research Coordinator manages daily trial operations, patient recruitment, and data collection. Both roles are essential in clinical research but differ in responsibilities and qualifications.

What cities are hiring for Clinical Research Doctor jobs?

Cities with the most Clinical Research Doctor job openings:

What states have the most Clinical Research Doctor jobs?

States with the most job openings for Clinical Research Doctor jobs include:

What are popular job titles related to Clinical Research Doctor jobs?

For Clinical Research Doctor jobs, the most frequently searched job titles are:

Clinical Research Doctor jobs near you

Clinical Research Nurse

Secaucus, NJ • On-site

Frontage Laboratories
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Frontage Laboratoriesexternal

$45 - $55/hr

Other

Re-posted 15 days ago

Key responsibilities

  • Assist Clinical Study Coordinators and perform study procedures such as venipunctures, biological specimen collection, vital signs, and safety assessments under supervision.

  • Record, evaluate, and review study data for accuracy and completeness, and develop strategies for implementing study procedures in compliance with protocols.

  • Support adverse event reporting, assist in informed consent processes, screen research subjects for eligibility, and maintain study-related documentation and supplies.

Job description

Clinical Research Nurse (per diem)


Title: Clinical Research Nurse (per diem)

Location: Secaucus, NJ (On-site required)

Reports To: Executive Medical Director and Principal Investigator


Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position Summary:

We are seeking a licensed and detail-oriented Clinical Research Nurse in support of clinical trials conducted at Frontage Clinical Services. in support of clinical trials conducted at Frontage Clinical Services. responsible for working under the guidance of the Investigators; Management, Study Coordinator and Supervisor, to perform study procedures required in clinical studies conducted on behalf of sponsors at the Frontage Clinical Services site in Secaucus.

 Responsibilities:

  • Assist Clinical Study Coordinators in any task as needed. 
  • Administer Medications (including IV administration route) per doctor’s and protocol instructions. 
  • Perform study procedures (e.g., venipunctures, obtain and process biological specimen samples, vital signs, safety assessments, etc.) as required by study protocol under the supervision of the Principal Investigator and Sub-Investigators, Director, Associate Director, and Clinical Research Coordinators.
  • Record study data in the source documents. Evaluate and review study data to ensure accuracy and completeness.
  • Develops a high level of familiarity and knowledge of the study protocol and flow chart of study procedures.  
  • Develops a strategy for implementing study procedures in compliance with the study protocol.  
  • Assists the Principal Investigator with gathering and recording relevant data for adverse event reporting and expedited reporting of serious adverse events to the sponsor. 
  • Responsible for maintaining emergency medication in the crash cart.
  • Assists in the administration of informed consent to research subjects under the supervision of the Principal Investigator.
  • Assists in the screening of research subjects to evaluate their eligibility for a clinical study.
  • Creates and performs QC procedures.
  • Assists in the reconciliation of IPs and maintaining accountability.
  • Acts independently to determine methods and procedures on new assignments and may supervise the activities of other Clinical Services personnel (e.g., Laboratory and Medical Technicians/ Assistants, Administrative Assistants, and Recruiters.)
  • Shows desire and initiative to increase knowledge and skills in clinical research.


Education and Requirements:

  • Bachelors in Science in Nursing.  
  • Registered Nurse in the State of New Jersey
  • Good communication skills with the ability to interact with the Principal Investigator, Sub-Investigators, and Frontage Clinical Services and sponsor personnel.
  • 1-3 years' experience in clinical research is desirable.  Knowledge of FDA regulatory requirements is necessary, or mandatory on-job training will be required.


Salary: $45-$55/hour


Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.