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Clinical Study Coordinator - RN job in Fairfield New Jersey | NEWS-Line for Family and General Medicine Practitioners

Clinical Study Coordinator - RN

Location:
Fairfield, New Jersey


Facility:
Consumer Product Testing Company


URL:



Email:
[email protected]

Fairfield, NJ

Clinical Study Coordinator - RN
CLN205

Job Type: Full Time. Base Hours: 9:00AM – 6:00PM Monday through Friday

The Clinical Study Coordinator position is based within our Human Clinical Evaluations department, and works with the Principal Investigator in the implementation of clinical trials.

MINIMUM QUALIFICATION REQUIREMENTS
To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and experience requirements.

ESSENTIAL DUTIES AND RESPONSIBILITIES

•Review of protocols, test samples, inclusion/exclusion criteria, recruitment requirements and study schedule.

•Implementation of all aspects of clinical trials, including compliance to Standard Operating Procedures, IRB approved protocols, Human Subject Protection, and regulatory requirements.

•Perform CRF transcription and data entry into Excel or EDC platform.

•Peer review clinical trial data as required for accuracy, data integrity, and protocol compliance

•Draft Final Reports, Data Summaries, and associated documentation.

EDUCATION and/or EXPERIENCE

•Must have RN and/or BSN with active license in NJ

•Must have four (4) years in medical, research or related field experience.

•Knowledge of Good Clinical Practices, FDA and HIPAA regulations, and product safety testing is preferable.

COMMUNICATION SKILLS

•Evidence of a strong communication and interpersonal skills with the ability to facilitate multi-disciplinary teams.

OTHER KNOWLEDGE, SKILLS and ABILITIES

Must have initiative and problem solving / analytical skills and keen attention to detail

•Must have proficient computer skills in the following: Windows Word, and Excel

•Must be organized, flexible, and able to work independently.

•Applicant should possess the ability to organize and maintain all clinical trial information for assigned projects and ensure adherence to established policies and procedures.

•Must have the ability to work collaboratively and effectively with other clinical team members and physicians.

PHYSICAL REQUIREMENTS
On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch; talk, hear, and smell. This position requires the ability to lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently.

Please send CV to [email protected]

All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age or any other characteristic protected by law.


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