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Whether you are healthy, or have a specific illness, we'll connect you with the right trial. Potentially get paid to access the most cutting edge medicines combating your disease. Most trials don't require much effort and will be located near you.

Certified Clinical Research Professional or Certified Clinical Research Professional or Certified Clinical Research Coord. The Clinical Research Nursing Instructor is responsible for the orientation, continuing education, staff development and continuous process improvement of clinical research n...

As the leading academic health system in New Jersey, we advance innovative strategies in high-quality patient care, education, and research to address both the clinical and social determinants of health. Five (5) years in acute care clinical services. Two (2) years in EBP and Research. Visible an...

The Patient Care/Clinical Research Registered Nurse is a hybrid position that provides patient care and case coordination to persons with HIV infection including pre and post test counseling, education of patient, family/significant others, staff and community. Ability to relate effectively to al...

Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH...

The Clinical Research Nurse carries out the research and works under the general supervision of the principal investigator responsible for the clinical trials. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies...

OTC product testing, or clinical research preferred but not required. Photoprotection - US Clinical & Instrumental Evaluation Intelligence Team. We are looking for a detail-oriented and proactive Studies Coordinator to join our Photoprotection US Clinical & Instrumental Evaluation Intelligence T...

Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 2 years experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH...

We are looking for a per diem Phlebotomist to join our Clinical Research Team. ...

Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within ...

The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance. Prefer 1 year of experience as a Care Access...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Under the direction of supervisor or designee, this position will ser...

Oncology clinical trials experience as a Clinical Research Coordinator (CRC) including experience(s) with an Investigational New Drug (IND) or Investigational Product (IP). As a Clinical Research Coordinator working at the Clifton, NJ site Monday - Friday you will be responsible for study coordin...

This individual will be responsible for managing clinical and non-clinical studies and assist with inventory management, labeling, returns and tracking shipping of clinical test materials. A client of ours in Florham Park, NJ is looking for a clinical research scientist to join their team. This i...

Reviews study with principal investigator and/or clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study. Recruits and evaluates potential study patients, and works w...

This role plays a pivotal role in assessing current and future status of existing affiliate clinical research programs and working together with the JTCC Oncology Clinical Research to further grow and expand such clinical research programs and participates in assessing, planning, implementing and...

The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. Works with Clinical Trial Oversight Managers (C...

The Oncology Clinical Research Nurse Solid Division is responsible for coordinating and overseeing clinical operations of a clinical trial and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research studies. Certified Clinical Research Professi...

Conceptually applies the research protocol to the clinical setting to allow accurate and timely completion of all duties. Maintains appropriate documentation associated with the assigned clinical study. Ensures studies are conducted according to established company policies and procedures as well...

Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Nurse carries out the research and works under the general supervision of the principal investigator responsible for the...

Requirements Medical license (MD, DO) - New Jersey 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator) Bilingual Spanish a plus Flexible hours - schedule can be tailored as required. Principal Investigator (MD/DO) The Principal Investigator will con...

Senior Clinical Research Associate. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a m...

Any other matters as assigned by management KNOWLEDGE & EXPERIENCE Education: Bachelors or Masters in Nursing Experience: Previous clinical research experience Nursing experience in a clinical setting Credentials: Current nursing licensure in good standing (Nurse practitioner) Knowledge and Skil....