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Description

Jefferson New Jersey location Responsibilities The Clinical Research Coordinator II works under limited supervision, assists with running clinical trials, completes regulatory documentation and tracks TJU IRB submission and approvals. May assist in the enrollment of human subjects. May provide clerical and technical support to ensure adherence to research protocols and quality of information received. • Performs a variety of research, data base, biospecimen collection and processing, as well as clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data. • Organizes and maintains documentation required for clinical trial(s). • Informs Principal Investigator and/or designated individual on any issues concerning patients response to treatment/medication/ any adverse effects overall to patients. • Assists Principal Investigator with regulatory body filings including IRB submissions. • May assist in the enrollment of human subjects. • May provide clerical and technical support to ensure adherence to research protocols and quality of information received.

Skills

Clinical Research Coordinator, Data, Data entry, Data collection, Data management, Patient recruitment, Clinical research, Patient records, Clinical trial, Edc, Oncology

Top Skills Details

Clinical Research Coordinator,Data,Data entry,Data collection

Additional Skills & Qualifications

Bachelor’s Degree with two years of clinical research experience; OR Master’s degree and one year of clinical research experience. OR High School with 8 years clinical research experience. OR High School with 6 years clinical research experience with a CRC certification from SoCRA or ACRP.

Experience Level

Intermediate Level

Pay and Benefits

The pay range for this position is $25.00 - $33.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Cherry Hill,NJ.

Application Deadline

This position is anticipated to close on Aug 7, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.