Top 9 Clinical research coordinator Jobs in Toms River Nj

Clinical Research Coordinator
Astera Cancer Care —Toms River, NJ
- $29 - $33 an hour
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Profit sharing
- Health savings account
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7d
Clinical Coordinator
Alliance Orthopedics —Freehold, NJ
- $45,000 - $55,000 a year
- Full-time
- Background check
- HIPAA
- Clinic experience
- Paid holidays
- Health insurance
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Administrative Clinical Coordinator - Patient Progression - F/T Nights
Hackensack Meridian Health —Neptune City, NJ
- $97,156.80 a year
- Full-time
- Nursing
- RN License
- BLS Certification
- Health insurance
- Dental insurance
Oncology Clinical Research Nurse - JS Hope Tower - F/T Days
Hackensack Meridian Health —Neptune City, NJ
- From $107,952 a year
- 8 hour shift
- Nursing
- RN License
- Customer service
- Health insurance
- Dental insurance
Clinical Care Coordinator RN - Home Care- Wall,NJ- FT
Hackensack Meridian Health —Wall, NJ
- From $92,144 a year
- 4 hour shift
- Nursing
- RN License
- BLS Certification
- Travel reimbursement
- Health insurance
Clinical Care Coordinator (Chiropractic & SoftWave)
New Hope Chiropractic —Tinton Falls, NJ
- $20 - $24 an hour
- Full-time
- Reliable transportation
- Communication skills
- Marketing
- Paid training
- Wellness program
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14d
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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Clinical Research Coordinator

Astera Cancer Care -
Toms River, NJ

Quick Apply

Job Details

Full-time
$29 - $33 an hour
7 days ago

Benefits

Profit sharing
Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching
Referral program

Qualifications

Collaborate with healthcare professionals
Informed consent
Filing
Mid-level
Research project coordination
Data integrity and documentation
Schedule management
Records management
Bachelor's degree
Clinical data entry
Data management
Informed consent procedures implementation
Oncology research
Research compliance clinical trial records management
Implementing research protocols
Patient recruitment
Communication with regulatory authorities for clinical trials
Oncology
Care coordination
Clinical consent forms
Ethical review application preparation
Pharmacy Technician Certification
Communication skills
Research compliance audit records management
Time management
Research compliance quality assurance records management

Full Job Description

Why Join Us?

For us, what matters most is excellence. We are caring professionals, people who live, work and dedicate themselves to the communities within New Jersey and Pennsylvania. As such, we strive to provide a sanctuary of excellence, precision, thoroughness and genuine compassion. We also take a whole-person approach to patient care and treatment, tailoring all that we do around their unique needs. And we do all we can for patients, going the extra mile to see that they’re supported, informed and getting the one-on-one care and service they deserve.

Job Description:

As an Oncology Clinical Research Coordinator (CRC), you will be an integral part of studies at Astera Cancer Care by recruiting participants, collecting and managing the study data for the successful management of clinical trials. This is a full-time position and the candidate MUST reside in New Jersey. The primary location for this role will be in Toms River, after the initial training period in East Brunswick, NJ.

Responsibilities Include:

Provide overall coordination of study-related activities for patients enrolled in cancer research studies through the Astera research program.
Coordinate with Principal Investigators, Supervisor and study sponsors and CROs to ensure that clinical research activities are performed in accordance with local and federal regulations and adhere to policies and procedures of Astera and the sponsors and CROs.
Assist in the coordination of tests and visits for patients and collaborate with the Astera study team to maximize work efficiency and productivity.
Assist in IRB submissions and interact with the Supervisor to maintain regulatory documents and administrative files for each protocol.
Work with research nurses, treating physicians, and Principal Investigators to confirm that each patient meets eligibility criteria specified for protocols and enrollment into clinical trials.
Maintain patient and regulatory research records.
Confer with all members of the clinical team to confirm appropriateness and timeliness of tests.
Collect follow-up data on patient’s post-treatment as required by the protocol.
Submit weekly reports to Supervisor, tracking patient screening/enrollment and subject status.
Enter research data into a centralized database as per protocol requirements.
Attend investigator meetings as required or requested by the Principal Investigator.
Prepare other study materials as requested by the Principal Investigator such as informed consent documents, case report forms, enrollment logs and drug/device accountability logs.
If applicable, able to prepare blinded and unblinded study drugs.
If applicable, act as primary coordinators for unblinded team.

Qualifications:

A Bachelor’s degree or equivalent working experience required.
Must reside in NJ.
Pharmacy Technician certified with infusion drug preparation training preferred.
At least one (1) year of clinical research experience, Oncology experience a plus.
Experience in Oncology Patient Recruitment and retention skills.
Experience with EDC, IWRS. CRF and Microsoft applications.
Able to travel between offices within the offices in Northeast Jersey area.
Excellent communication skills.
Excellent time management skills.

Pay Range: $29/hr - $33/hr

Pay Transparency: The above reflects the anticipated pay range for this position. The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills and professional experience.

We are proud to offer a comprehensive benefit package and paid time off. The health benefits include immediate eligibility for medical, dental, vision, life, disability, HSA, FSA and other ancillary benefits. We also offer a 401(k) plan with company contribution, profit sharing, tuition assistance and employee referral bonus.

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Refine Your Search

clinical research coordinator jobs in toms river nj

Clinical Research Coordinator

Clinical Coordinator

Administrative Clinical Coordinator - Patient Progression - F/T Nights

Oncology Clinical Research Nurse - JS Hope Tower - F/T Days

Clinical Care Coordinator RN - Home Care- Wall,NJ- FT

Clinical Care Coordinator (Chiropractic & SoftWave)

Clinical Donation Coordinator I - PeeDee Region

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