Top 1087 Research Jobs in New Jersey

Clinical Research Coordinator I
Rare Disease Research, LLC —Iselin, NJ
- $24 - $31 an hour
- 8 hour shift
- Background check
- Vital signs
- Bachelor of Science
- Health insurance
- Dental insurance
Quick Apply
17h
Clinical Research Coordinator I
SGS —Union, NJ
- $22 - $23 an hour
- Full-time
- Computer literacy
- Basic math
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I
Hassman Research Institute, LLC —Marlton, NJ
- $26.09 - $33.32 an hour
- Blood sampling
- Vital signs
- Psychiatry
- Health insurance
- Dental insurance
Quick Apply
Research Project Coordinator II
Rutgers University —New Brunswick, NJ
- $59,893.48 a year
- Full-time
- Writing skills
- Mid-level
- Master's degree
- Paid holidays
- Dental insurance
1d
Research Associate II
Rutgers University —Newark, NJ
- $65,272 a year
- Full-time
- Mid-level
- 3 years
- Master's degree
- Paid holidays
- Dental insurance
Research Assistant (Multiple Vacancies)
Rutgers University —Newark, NJ
- $18 - $35 an hour
- Part-time
- Computer literacy
- Administrative experience
- University
- Paid holidays
- Dental insurance
Research Project Assistant
Rutgers University —New Brunswick, NJ
- $52,602.48 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Computer literacy
- Paid holidays
- Dental insurance
Temporary Research Assistant (Logistics)
Rutgers University —Newark, NJ
- $15.92 - $150.00 an hour
- Part-time
- Bachelor of Science
- Mid-level
- Clinic
- Paid holidays
- Dental insurance
7d
Clinical Research Associate
Rutgers University —Newark, NJ
- $68,147 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Paid holidays
- Dental insurance
Research and Development Scientist 1
Keystone Industries —Gibbstown, NJ
- $60,000 - $80,000 a year
- Monday to Friday
- Computer literacy
- Basic math
- Maintenance
Quick Apply
8d
Data Coordinator I
Columbia University —Fort Lee, NJ
- $66,300 - $68,000 a year
- Full-time
- Hybrid work
- Computer literacy
- HIPAA
- Bachelor's degree
Research Scientist
Hudson Valley Technical Solutions —Montvale, NJ
- $76,920.05 - $92,634.91 a year
- Contract
- Mid-level
- Bachelor's degree
- In-person
Quick Apply
Research Regulatory Coordinator, Full Time,
Virtua Health —Moorestown, NJ
- $26.00 - $39.11 an hour
- Full-time
- Mid-level
- Office
- Organizational skills
- AD&D insurance
- Disability insurance
5d
Clinical Research Coordinator
Hackensack Meridian Health —Hackensack, NJ
- From $83,782.40 a year
- Full-time
- Customer service
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Temporary Research Assistant
Rutgers University —Piscataway, NJ
- $30 an hour
- Part-time
- Mid-level
- Databases
- Analysis skills
- Paid holidays
- Dental insurance
Research Assistant
Rutgers University —Piscataway, NJ
- From $14,280 a year
- Part-time
- Computer science
- Computer Science
- Bachelor of Science
- Paid holidays
- Dental insurance
Research Program Coordinator, Research Clinical-Trials, Full Time, Day
Valley Health System of Ridgewood NJ —Paramus, NJ
- $30.82 - $38.53 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Hospital
- Commuter assistance
- AD&D insurance
Chemist-Chemaid Research & Development Salaried SG&A
kdc/one —Saddle Brook, NJ
- $72,000 - $85,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Paid holidays
- Disability insurance
Quick Apply
14d
Temporary Research Assistant (Multiple Vacancies)
Rutgers University —Newark, NJ
- $15.92 - $18.00 an hour
- Part-time
- Adults
- Office
- Master's degree
- Paid holidays
- Dental insurance
Research Associate III
Woods Hole Oceanographic Institution —Clark, NJ
- $79,565 - $103,133 a year
- Full-time
- Analysis skills
- Doctor of Philosophy
- Travel
6d

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Clinical Research Coordinator I

Rare Disease Research, LLC
Iselin, NJ

Quick Apply

Job Details

Full-time
$24 - $31 an hour
17 hours ago

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Vital signs
Bachelor of Science
BLS Certification
Collecting samples for laboratory testing
Bachelor's degree
Training & development
Clinical trial support in drug product development

Full Job Description

About Rare Disease Research:

As an independent clinical research site, we are 100% dedicated to conducting clinical research, accelerating the development of safe and effective treatments and providing rare disease patients with access to innovative investigational therapies. We are a passionate, caring, multi-disciplinary team conducting clinical research with expertise and compassion, and always to the highest ethical standards.

About This Opportunity:

We are looking for a clinical research coordinator who has at least 2 years experience with the conduct of clinical research to join our wonderful team of motivated research professionals. Ideally, the right candidate has prior clinical research experience conducting investigational clinical trials and is already familiar with clinical research workflows, regulatory requirements, and data collection and documentation practices.

* Important Note: Applicants for employment in the United States must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States and with Rare Disease Research.

Responsibilities:

Assists Principal Investigator (PI) in protection of the rights and welfare of all human research participants involved in research in accordance with federal regulations and university and sponsoring agency policies and procedures.
Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.
Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
Collects documents needed to initiate the study and submit to the sponsor (e.g., Form FDA 1572, CVs, etc.).
Works with the PI to develop and implement recruitment strategies in accordance with HRPO (IRB) requirements and approvals.
Conducts or participates in the informed consent process including interactions with the HRPO (IRB) and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.
Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
Performs safety and efficacy assessments per study protocol.
Collect or coordinate collection of clinical procedures such as vital signs, ECGs, blood draws, IP infusions.
Responsible for timely data entry and query resolutions.
Reports study findings, such as serious adverse events (SAEs) or protocol deviations (PDs) to the applicable department, such as the sponsor or IRB.
Manages participant chart binders and coordinates accurate completion of source with various delegated staff.
Follows participants from the start to end of study participation and escalates safety concerns to appropriate individuals, such as the PI or Medical Monitor.
Prepare study data for interim monitoring visits and meet with study monitor to follow-up on resolving queries/issues.
Communicate with sponsors, CROs, vendors, or other representatives promptly and professionally.
Completes study documentation and maintains study files in accordance with sponsor requirements and University policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
Updates source documents per study protocol amendment.
Coordinate operations with other departments to facilitate completion of procedures during participant visits, includes communications with nurse practitioners, medical assistants, pharmacy, regulatory, and/or physical therapy.
Retains all study records in accordance with sponsor requirements.
Works with the PI and study-specific RAs to manage the day to day activities of the study including problem solving, communication, and protocol management.
Ability to exercise independent judgment and discretion

The above statements are intended only to describe the general nature of the job, and should not be construed as an all-inclusive list of position responsibilities.

Requirements:

BA/BS in a life sciences or related field required.
2 years previous CRC experience at a clinical trial site
Strong phlebotomy skills
Must have GCP, IATA, ALCOAC training
BLS/CPR training upon hire date

Job Type: Full-time

Salary: $24-31/hour

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Schedule:

8 hour shift
Day shift
Monday to Friday

Ability to commute/relocate:

Iselin, NJ 08830: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

Have you received the COVID 19 vaccinations or would you be willing to do so before beginning employment?

Work Location: One location, on site and in person

Rare Disease Research is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, or any other characteristic protected by federal, state or local laws.

Notice To Third-Party Agencies:

Rare Disease Research does not accept unsolicited resumes from recruiters or agencies. Any staffing/employment agency, person or entity that submits an unsolicited resume to this site does so with the understanding that the applicant's resume will become the property of Rare Disease Research will have the right to hire that applicant at its discretion and without any fee owed to the submitting staffing/employment agency, person, or entity.

Job Type: Full-time

Pay: $24.00 - $31.00 per hour

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

research jobs in new jersey

Clinical Research Coordinator I

Clinical Research Coordinator I

Clinical Research Coordinator I

Research Project Coordinator II

Research Associate II

Research Assistant (Multiple Vacancies)

Research Project Assistant

Temporary Research Assistant (Logistics)

Clinical Research Associate

Research and Development Scientist 1

Data Coordinator I

Research Scientist

Research Regulatory Coordinator, Full Time,

Clinical Research Coordinator

Temporary Research Assistant

Research Assistant

Research Program Coordinator, Research Clinical-Trials, Full Time, Day

Chemist-Chemaid Research & Development Salaried SG&A

Temporary Research Assistant (Multiple Vacancies)

Research Associate III

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