Clinical Research Coordinator
Clinical Research Coordinator
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Job Description
Description
Title: Clinical Research Coordinator Norwalk Hospital Cancer Research Full time 40 hours Monday Friday 8:00am to 4:30pm
Summary: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Responsibilities include; patient screening and recruitment coordination of care of the research patient protocol implementation data collection and query resolution and submission to the Institutional Review Board (IRB). Coordinates studies in Oncology therapeutic areas. Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations
Responsibilities:
1.Screens patients for study participation e.g. reviews medical record collaborates with medical & research staff etc. and procures informed consent.
2. Maintains accurate and thorough documentation on all source documents and case report forms (CRFs) for each study patient. Resolves all patient queries.
3. Maintains communication with investigators/researchers patients internal and external collaborators (e.g. consulting physicians) sponsors federal regulatory agencies and other involved parties as required.
4. Participates in investigator coordinator or study initiation meetings accordingly. Coordinates and participates in monitoring visits/audits with regulatory agencies or sponsors.
5. Maintains current regulatory (GCP HSR) and study specific required trainings.
6. Prepares and submits all study protocols consent forms and other required documents to the Institutional Review Board (IRB).
7. Educates hospital staff about protocols through inservices written materials and oneonone interaction for each study and each patient and for general marketing.
8. Demonstrates flexibility in daily routine and effectively accommodates for the needs of the job (e.g. early or late patient enrollment).
9. Performs procedures including EKG Phlebotomy blood and body fluid sampling packing and shipment of human samples body measurements and examinations within scope of practice and training consistent with clinic and study specific policies/procedures and scope of care under the guidance of the supervisor.
10. Fulfills all compliance responsibilities related to the position.
11. Maintain and Model Nuvance Health Values.
12. Demonstrates regular reliable and predictable attendance.
13. Performs other duties as required.
Other Information:
- Bachelor Degree OR Allied Health Professional Degree AND three years jobrelated experience.
- Minimum 1year clinical experience in medical field.
- PREFER: Clinical Research experience
- Fluency in medical terminology.
- Knowledge of clinical trials research and general medicine.
- Strong computer skills.
- Strong attention to detail and organizational skills
- Outstanding interpersonal skills
- Basic Life Support current or willing to take course
- Valid Drivers license
- PREFER: Professional research certification
- PREFER: Basic Life Support
Department: Cancer Research
Exempt: Yes
Salary Range: $28.78 $53.45 Hourly commensurate with experience.
Required Experience:
IC
Employment Type
Full Time
