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Clinical Research Jobs in Rutherford, NJ (NOW HIRING)

Care Access

Clinical Research Assistant

Yonkers, NY · On-site

$19 - $33/hr

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

ABOUT VITALIEF Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider (FSP) solutions to ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

ABOUT VITALIEF Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider (FSP) solutions to ...

Actalent

Clinical Research Coordinator

Edison, NJ

$32 - $35/hr

Clinical Research Coordinator We are seeking a dedicated Clinical Research Coordinator to join our team. In this role, you will assist in literature reviews, proposal development, and oversee various ...

Apply Early

Actalent

Clinical Research Coordinator

Edison, NJ · On-site

$32 - $35/hr

Clinical Research Coordinator We are seeking a dedicated Clinical Research Coordinator to join our team. In this role, you will assist in literature reviews, proposal development, and oversee various ...

Apply Early

Actalent

Clinical Research Coordinator

Edison, NJ

$32 - $35/hr

Clinical Research Coordinator We are seeking a dedicated Clinical Research Coordinator to join our team. In this role, you will assist in literature reviews, proposal development, and oversee various ...

Apply Early

NYULMC

Program Lead, Clinical Research

New York, NY · On-site

In this role, the successful candidate The Clinical Translational Science Institute (CTSI), Clinical Research Centers (CRC) is seeking a highly motivated and organized individual to join our ...

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Showing results 1-20

All JobsClinical Research JobsClinical Research Jobs in Rutherford, NJ

Clinical Research information

See Rutherford, NJ salary details

$50K

$109.4K

$192.7K

How much do clinical research jobs pay per year?

As of Jul 3, 2026, the average yearly pay for clinical research in Rutherford, NJ is $109,422.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,600.00 and $124,900.00 per year, depending on experience, location, and employer.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

What Are Different Clinical Research Jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in Clinical Research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What is the starting salary in clinical research?

The starting salary for a clinical research associate or coordinator typically ranges from $50,000 to $65,000 annually, depending on location, education, and experience. Entry-level roles often require knowledge of Good Clinical Practice (GCP) and familiarity with clinical trial management systems.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, often followed by a master's or doctoral degree for advanced roles. Gaining experience in clinical settings, understanding regulatory requirements, and obtaining certifications like the Certified Clinical Research Professional (CCRP) can enhance job prospects.

Which clinical research jobs pay the most?

Senior roles in clinical research, such as Clinical Project Managers, Clinical Directors, and Principal Investigators, tend to have the highest salaries. These positions often require extensive experience, advanced degrees, and certifications like CCRP or RAC, and they typically involve overseeing multiple studies or teams in a regulatory-compliant environment.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulations, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail and knowledge of Good Clinical Practice (GCP) are essential.

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

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.
More about Clinical Research jobs
What are the most commonly searched types of Clinical Research jobs in Rutherford, NJ? The most popular types of Clinical Research jobs in Rutherford, NJ are:
What job categories do people searching Clinical Research jobs in Rutherford, NJ look for? The top searched job categories for Clinical Research jobs in Rutherford, NJ are:
What cities near Rutherford, NJ are hiring for Clinical Research jobs? Cities near Rutherford, NJ with the most Clinical Research job openings:
Clinical Research jobs near you
Infographic showing various Clinical Research job openings in Rutherford, NJ as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $109,422 per year, or $52.6 per hour.
Clinical Research Scientist

Clinical Research Scientist

Mitsubishi Tanabe Pharma America

Jersey City, NJ • On-site

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 22 days ago

Job description

Company Description
Entrepreneurial
Spirit, Rooted in Tradition. At Mitsubishi Tanabe Pharma Development America (MTDA), we can tout a storied reputation more than 300 years in the making. Our parent company, Mitsubishi Tanabe Pharma Corporation (MTPC), is a research-driven pharmaceutical company with global reach - and one of Japan's
oldest and most respected companies.
Relatively new to the U.S. market, the innovative compounds of the Mitsubishi Tanabe Pharma Group have already enjoyed commercial success under the brand labels of our U.S. partners. In this next phase of development, we plan to bring exciting new compounds to market under our own MT Pharma America label. We're currently building a new commercial organization and expanding our other functions to support this strategy.
Reporting to the Senior Director, Clinical Development, the Clinical Research Scientist will provide
leadership in the direction, planning, execution, and interpretation of clinical protocols, research, data collection activities, and clinical operations. He/she will establish and approve scientific methods for design and implementation of clinical protocols and final reports. Incumbent will work with others to develop statistical plans and perform data analysis of completed clinical trials. The incumbent will support new and ongoing clinical research and clinical trials and ensure efficient and timely processing of Confidential Disclosure Agreements and Clinical Trial Agreements. Monitors adherence to protocols and determines study completion.
The Clinical Research Scientist may interact with Investigational sites, clinical consultants, CRO's and other vendors. He/she will provide clinical research in therapeutic areas for purposes of Regulatory submissions and product selection and development. He/she will work directly with senior program leadership and with KOLs, investigators and CROs externally to design, execute, analyze and interpret the studies for which they are responsible.
Job Description
  • Prepare clinical-related documents with minimal supervision and routine documents independently as directed. Examples include, protocol synopses, protocols, CRFs, and supporting work for regulatory
    submissions such as INDs.
  • Author abstracts and manuscripts for publication in peer-reviewed journals.
  • Evaluate and select potential investigative sites in collaboration with Clinical Operations staff.
  • Ability to prepare, present and defend complex aspects of protocol design and/or study data at
    investigator and internal meetings.
  • Oversee and coordinate the collection of and/or collect pre-study documents
  • Participate in data review and discrepancy resolution, team meetings/presentations with increasing
    levels of independence and support the Program Clinical Leader or Sr. Management as needed.
  • Assist in managing regulatory safety reporting with the following: SAE queries and follow-up,
    annual reports, investigator brochures, ability to learn various databases.
  • Critically review and synthesize complex information from reviews of the scientific and clinical
    literature.

Qualifications
  • Minimum 2-5 years of pharmaceutical industry clinical trial experience.
  • Experience in immunology or endocrinology therapeutic areas is a plus.
  • Primary experience with development of clinical trial protocols.
  • Medical or scientific writing experience a must and familiarity with clinically applied science or
    pharmaceutical development.
  • Good understanding of FDA regulatory, ICH, and GCP requirements.
  • Excellent communication skills, written and verbal.
  • Superior interpersonal communication and the ability to work across company disciplines and functional units.
  • Proven ability to simultaneously manage activities associated with multiple clinical trials and programs with short timelines.
  • Attention to detail and a commitment to high quality and on-time deliverables are key success factors.
  • Willingness to travel up to 30% domestically and internationally.

Additional Information
Our Value Proposition:
Enjoy the fast-moving, entrepreneurial spirit more typically found in a small biotech, complemented by the benefits of a global pharmaceutical/chemical conglomerate. At this time, Mitsubishi Tanabe Pharma America offers our employees unparalleled opportunities for career success coupled with a supportive level of employee benefits:
Medical/Dental Life Insurance / Supplemental Life Insurance/Dependent Life Insurance /Accidental Death & Dismemberment Insurance / Business Travel Accident Insurance / Short-Term Disability / Long-Term Disability / Flexible Spending Accounts / Employee's Savings Plan (401K Plan) / Competitive Paid Time Off

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