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Clinical Research Coordinator
2 months ago
Background:
Our organization is currently accepting applicants for the Clinical Research Coordinator position within our clinical research program. We are a private cardiology practice with over 20 doctors, six offices, and with privileges at four hospitals in Fairfield County. We have developed a clinical research program within our practice investigating new cardiovascular medications and devices that are in Phase II-IV trials.
Clinical Research Coordinators work hand in hand with the patients and physicians within our practice to facilitate the research work flow.
The position is a full time salaried position with benefits. There is an expected 40 hour a week requirement. The applicant must be able to work autonomously within our organization and must be detail-oriented.
Opportunities also include:
- Rounding/Shadowing with an interventional cardiologist
- Travel to Cardiology Conferences
- Working on our Cardiology Podcast, interviewing prominent physicians & researchers
- Working on all aspects of trials from the ground up: Startup, Regulatory Documentation, Generation of CRFs, IRB submissions, Monitoring visits, etc.
Responsibilities:
Carefully collect, compile and document clinical research data according to the study protocol and sponsor guidelines.
Maintain documentation according to protocols, standard operating procedures, and FDA requirements.
Perform administrative tasks for the clinical research department including filing, appointment scheduling, phone follow ups, mailings, supply inventory, investigational product inventory etc.
Screen patients to identify eligible study candidates through chart review, patient interviews, discussions with practice doctors, and other methods.
Facilitate enrollment of eligible patients by working closely with physicians and staff.
Explain studies to eligible candidates, answer questions, and obtaining written consent as delegated by the study PI.
Perform basic clinical evaluations: including blood pressure, pulse, performing EKGs, phlebotomy, review current and changes to medications, document adverse events.
Interface with study monitors to ensure proper trial conduct & documentation.
Assist the Manager of Clinical Research in developing and improving processes to optimize efficiency and effectiveness of clinical research department.
Perform all clinical research activities in accordance with Human Subject Protection rules and Good Clinical Practice guidelines.
Perform other related duties as assigned by the PIs and Manager of Clinical Research.
Skills:
Knowledge of basic medical terminology and clinical skills
Must have reliable personal transportation for regular transport between offices (within Fairfield County, CT)
Proficient with Microsoft office, general computer systems, and ability to learn other applications as needed
Excellent written and verbal communication skills
High level of organization, ability to multitask, ability to work as a team and independently
Experience:
Bachelor’s degree required
Previous clinical research experience strongly preferred
Other research experience, science background, or medical background preferred
Experience in cardiology preferred
For more information please visit our website: www.futurepulse.org
Job Type: Full-time
Pay: From $60,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Retirement plan
- Vision insurance
Schedule:
- 8 hour shift
Education:
- Bachelor's (Preferred)
Experience:
- Clinical Trials: 1 year + (Required)
- Clinical Research: 1 year + (Required)
- Work Location: In person