ZipRecruiter

Log In

2

Entry Level Clinical Research Jobs in Rutherford, NJ

Adams Clinical

Clinical Research Assistant

New York, NY · On-site

$24 - $30/hr

We are seeking entry-level applicants for the Clinical Research Assistant role at our Harlem location. This role is ideal for entry-level candidates interested in learning clinical research ...

Adams Clinical

Clinical Research Assistant

New York, NY · On-site

$24 - $30/hr

We are seeking entry-level applicants for the Clinical Research Assistant role at our Harlem location. This role is ideal for entry-level candidates interested in learning clinical research ...

Tang Capital

Biotechnology Research Analyst

Manhattan, NY · On-site

$120K - $210K/yr

Position Summary Tang Capital is seeking an entry-level Biotechnology Research Analyst to join its New York office. The Analyst will support scientific, clinical, and strategic analyses across ...

MicroCoders LLC

QA/BA Positions

New York, NY

... and Clinical Research. Within our staffing offering, we provide temporary, temporary-to-hire ... MicroCoders LLC is actively looking candidates for Jr./Entry level QA analyst position with our ...

MicroCoders LLC

QA/BA Positions

New York, NY · On-site

... and Clinical Research. Within our staffing offering, we provide temporary, temporary-to-hire ... MicroCoders LLC is actively looking candidates for Jr./Entry level QA analyst position with our ...

Genesis Global Group

Be Seen First

Entry Level Account Manager-Queens, NY

Queens, NY · On-site

$45K/yr

... a CLIA certified clinical laboratory with multiple state licensing, specializing in ... Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis ...

next page

Showing results 1-20

All JobsClinical Research JobsEntry Level Clinical Research JobsEntry Level Clinical Research Jobs in Rutherford, NJ

Entry Level Clinical Research information

See Rutherford, NJ salary details

$8

$23

$47

How much do entry level clinical research jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for entry level clinical research in Rutherford, NJ is $23.15, according to ZipRecruiter salary data. Most workers in this role earn between $17.64 and $26.44 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of an entry level clinical research?

In an entry level clinical research position, your day-to-day tasks may include collecting and entering study data, helping prepare regulatory documentation, monitoring study progress, and ensuring strict protocol compliance. You’ll often assist with scheduling participant visits, communicating with study subjects, and supporting senior clinical research staff. Collaboration is frequent, as you may work closely with coordinators, principal investigators, and other healthcare professionals. This hands-on experience provides a valuable foundation for understanding the research process and can open doors for career advancement in clinical research.

How to start a career in entry level clinical research?

To start a career in entry level clinical research, obtain a relevant bachelor's degree such as in life sciences, healthcare, or related fields. Gaining knowledge of Good Clinical Practice (GCP) guidelines, developing strong organizational skills, and seeking internships or entry-level positions can help build experience in clinical trial processes and regulatory requirements.

What is an entry level clinical research?

An Entry Level Clinical Research job involves assisting in the planning, execution, and monitoring of clinical trials that test the safety and effectiveness of new treatments or medical devices. Responsibilities may include data collection, documentation, regulatory compliance, and supporting senior researchers. These roles are typically found in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. Strong attention to detail, organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines are important for success. This position serves as a stepping stone for careers in clinical research, regulatory affairs, or healthcare innovation.

Is it hard to get into entry level clinical research?

Entry level clinical research positions typically require a relevant degree such as a bachelor's in life sciences or healthcare, along with strong organizational and communication skills. While competition can vary, gaining certifications like the Certified Clinical Research Professional (CCRP) can improve job prospects, and some roles may offer on-the-job training for candidates with related backgrounds.

What are the key skills and qualifications needed for an entry level clinical research?

To thrive as an Entry Level Clinical Research professional, you generally need a bachelor’s degree in a life science or health-related field, strong attention to detail, and basic understanding of clinical trial processes. Familiarity with data entry systems, electronic data capture (EDC) platforms, and adherence to Good Clinical Practice (GCP) guidelines or certificates are often expected. Excellent organizational skills, effective communication, and a collaborative mindset help you stand out in this position. These skills ensure accurate data collection, regulatory compliance, and successful teamwork within complex research environments.

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 Entry Level Clinical Research jobs in Rutherford, NJ look for?

The top searched job categories for Entry Level Clinical Research jobs in Rutherford, NJ are:

What cities near Rutherford, NJ are hiring for Entry Level Clinical Research jobs?

Cities near Rutherford, NJ with the most Entry Level Clinical Research job openings:

Entry Level Clinical Research jobs near you
Infographic showing various Entry Level Clinical Research job openings in Rutherford, NJ as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $48,159 per year, or $23.2 per hour.

Clinical Research Assistant

Adams Clinical

New York, NY • On-site

$24 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

Join Us in Shaping the Future of Clinical Research
Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values-Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration-we create an environment where meaningful work drives meaningful change.
At Adams Clinical, you'll find:
  • A culture of respect, transparency, and continuous improvement
  • Opportunities for professional growth and learning
  • A team dedicated to improving lives through innovation and integrity

If you're passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we'd love to have you on our team.
Overview
Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions, supporting both inpatient and outpatient studies.
We are seeking entry-level applicants for the Clinical Research Assistant role at our Harlem location. This role is ideal for entry-level candidates interested in learning clinical research operations, contributing to study execution, and developing foundational skills in patient interaction, data management, and regulatory compliance.
The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical trials at the site level. Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. This role is an ideal entry point for individuals seeking to gain hands-on experience in clinical research.
Key Responsibilities
  • Support study start-up activities, including supply inventory, document preparation, and site initiation readiness.
  • Assist with participant screening workflows as delegated, including scheduling screening visits and collecting basic information such as demographics, medical history, and other study-relevant details to support eligibility assessment.
  • Schedule and prepare for participant visits, including source prep, lab kits, and CRFs.
  • Serve as a participant liaison-confirm appointments, coordinate transportation, and maintain ongoing communication.
  • Escort and assist participants during on-site visits; perform vital signs, ECGs, and specimen collection/processing as trained.
  • Complete accurate, ALCOA+-compliant source documentation for delegated procedures.
  • Perform data entry into EDC systems and assist with query resolution.
  • Maintain study binders, charts, and logs; support supply management.
  • Ensure accurate capture and upload of paper source documents into eSource systems in accordance with site processes and regulatory requirements, supporting long-term retention and audit readiness.
  • Obtain, track, and manage medical releases, as well as medical and pharmacy records from external providers as needed, in accordance with site SOPs and protocol requirements.
  • Support CRCs during monitoring visits and assist with preparing documentation and materials to ensure audit and inspection readiness.
  • Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.
  • Develop proficiency in site SOPs, institutional policies, and GCP requirements to build foundational knowledge in compliant research practices.
  • Assist in collecting and entering study data into trackers, logs, and EDC systems, focusing on accurate and timely data collection.
  • Support CRCs in maintaining accurate records and updating study metrics.

Qualifications
  • Minimum requirement of a high school diploma or GED equivalent; Bachelor's degree preferred.
  • No prior clinical research experience is necessary; training will be provided. Basic understanding of clinical research principles is a plus.
  • Strong attention to detail, organization, and communication skills.
  • Proficiency in Microsoft Office.
  • Willingness to perform phlebotomy and clinical procedures as trained.

Pay: $24.00 - $30.00 per hour
Benefits:
  • 401(k) matching
  • Medical, Dental, & Vision insurance
  • Employee assistance program
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Parental leave
  • Professional development assistance

Adams Clinical is committed to being an equal opportunity and affirmative action employer. We focus on hiring and nurturing top talent. All employment decisions, including recruitment, hiring, promotion, compensation, transfer, training, discipline, and termination, are made based on the candidate's or employee's qualifications relevant to the position. These decisions are made without regard to age, sex, sexual orientation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected status.
In compliance with federal law, all individuals hired must, as a condition of employment, provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the required timeframe. Adams Clinical participates in E-Verify to confirm employment eligibility.

Apply