Clinical Research Coordinator - Danbury, CT (On-site)

Community Options, Inc.; Danbury (CT); On-site; Full time

Job summary

A leading company in healthcare is seeking a Clinical Research Coordinator in Danbury, CT. The role involves coordinating clinical research studies, including patient recruitment, data management, and regulatory compliance. Ideal candidates will possess a Bachelor’s degree and relevant experience, with a strong focus on interpersonal communication and attention to detail.

Qualifications

• Bachelor’s Degree, Allied health professional degree, or equivalent.
• 1-2 years’ experience with EDC and CRFs.
• Basic Life Support (BLS) certified or willing to obtain.

Responsibilities

• Screens patients for study participation, maintains accurate documentation.
• Coordinates studies in Oncology therapeutic areas, collaborates with investigators.
• Maintains communication with all involved parties during the study process.

Skills

Medical Terminology

Interpersonal Communication

Attention to Detail

Organizational Skills

Education

Bachelor’s Degree or Allied Health Degree

Job description

Clinical Research Coordinator - Danbury, CT (On-site)

Clinical Research Coordinator - Danbury, CT (On-site)

4 days ago Be among the first 25 applicants

Description

Clinical Research Coordinator - Danbury Hospital (On-site)

Full-time, 40 hours; Monday - Friday, 8:00 am - 4:30 pm

Summary

Reports to Director of Clinical Trials or Clinical Research Nurse Lead: 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

Description

Clinical Research Coordinator - Danbury Hospital (On-site)

Full-time, 40 hours; Monday - Friday, 8:00 am - 4:30 pm

Summary

Reports to Director of Clinical Trials or Clinical Research Nurse Lead: 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

Major Accountabilities:

• Screens patients for study participation e.g. reviews medical record, collaborates with medical & research staff, etc. and procures informed consent.,
• Maintains accurate and thorough documentation on all source documents and case report forms (CRFs) for each study patient. Enters data. Resolves all patient queries.
• Maintains communication with investigators/researchers, patients, internal and external collaborators (e.g. consulting physicians, Monitors), sponsors, federal regulatory agencies, and other involved parties as required.
• Participates in investigator, coordinator, or study initiation meetings accordingly. Coordinates and participates in monitoring visits/audits with regulatory agencies or sponsors.
• Maintains current regulatory (GCP, HSR) and study specific required trainings.
• Prepares and submits all study protocols, consent forms, and other required documents to the Institutional Review Board (IRB).
• Educates hospital staff about protocols through in-services, written materials and one-on-one interaction, for each study and each patient, and for general marketing.
• Demonstrates flexibility in daily routine and effectively accommodates for the needs of the job (e.g. early or late patient enrollment).
• 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.
• Fulfills all compliance responsibilities related to the position.
• Performs other duties as assigned.
  
  

Requirements

• Bachelor’s Degree, Allied health professional degree, or equivalent experience.
• Minimum of one-two (1-2) years’ experience with EDC and CRFs.
• Minimum Knowledge, Skills and Abilities Requirements:Ability to multi-task and work as a team and independently.
• Knowledge of Medical Terminology, good clinical practice, FDA, OHRP, and HIPAA policies.
• Outstanding interpersonal communication skills.
• Strong attention to detail, self-motivation, and good organizational skills.
• Ability to prioritize quickly and follow directions and protocol.
  
  

License, Registration, Or Certification Requirements

• Basic Life Support (BLS) certified or willing to obtain upon employment. Valid driver’s license and reliable transportation. PREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Oncology experience is a plus.
  
  

Department: Cancer Research

Exempt: Yes

Salary Range: $27.91 - $51.83 Hourly, commensurate with experience.

About Nuvance Health

Nuvance Health has a network of convenient hospital and outpatient locations — Danbury Hospital, New Milford Hospital, Norwalk Hospital and Sharon Hospital in Connecticut, and Northern Dutchess Hospital, Putnam Hospital Center and Vassar Brothers Medical Center in New York — plus multiple primary and specialty care physician practices locations, including The Heart Center, a leading provider of cardiology care. Non-acute care is offered through various affiliates.

EOE, including disability/vets.

We will endeavor to make a reasonable accommodation to the known physical or mental limitations of a qualified applicant with a disability unless the accommodation would impose an undue hardship on the operation of our business. If you believe you require such assistance to complete this form or to participate in an interview, please contact Human Resources at 203-739-7330 (for reasonable accommodation requests only). Please provide all information requested to assure that you are considered for current or future opportunities.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Other

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care

Referrals increase your chances of interviewing at Community Options, Inc. by 2x

Get notified about new Clinical Research Coordinator jobs in Danbury, CT.

Clinical Research Coordinator - Danbury, CT (On-site)

Principal Pharmacovigilance Safety Study Coordinator

Clinical Care Coordinator (PT, OT, RN) - HomeCare

Patient Access Associate II Full Time 1st Shift CFC

Clinical Education Coordinator Respiratory Services and Neu

Clinical Care Coordinator (PT, OT, RN) - HomeCare

Clinical Coordinator (RN) - Norwalk Hospital Wound Care - Per Diem

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.