Top 7918 Protocol coordinator Jobs

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Clinical Research Coordinator III

System One -
Carnegie, PA

Quick Apply

Job Details

Contract

Qualifications

Staff supervision
Informed consent
Bachelor of Science
Mid-level
3 years
Clinical research protocol review
Research project coordination
Interview research
Bachelor's degree
Clinical data entry
Informed consent procedures implementation
Data entry
Interviewing
Implementing research protocols
Patient recruitment
Communication with regulatory authorities for clinical trials
Patient progress monitoring
Patient interaction
Certified Risk Coder (CRC)
Data collection
IRB compliance
Training
Ordering supplies
Ethical review application preparation

Full Job Description

Job Title: Clinical Research Coordinator III
Location: Pittsburgh, PA, Hybrid: Combination of On-Campus or Remote determined by the department.
Schedule: Varied based on participants schedule
Type: Direct Hire or 6 -12 month Contract based on department needs

Overview:
A top-ranked research university is currently searching for a Clinical Research Coordinator III for one of its growing departments to be for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process.

Responsibilities:

Will work closely with the Principal Investigators (PIs), study staff and clinical staff.
Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes.
Conduct and is responsible for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process.
Encouraged to prepare strategies to improve enrollment/retention. May need to maintain and order supplies as needed.
Will Assess protocol feasibility and establish protocol-specific recruitment plans.
May be required to train junior staff and oversee the work of others as directed.
Will be required to communicate effectively with study participants and potential community recruits.
Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols.
Recruits research subjects and conducts interviews and research assessments.

Requirements:

Minimum Education Requirement: Bachelor’s Degree
Experience Requirement: At least 3-5 years of clinical trial/clinical research experience within industry/sponsor trials
Education/Experience Substitution: A combination of relevant education and experience will be considered in place of the specified educational and/or experience requirements.
Preferred Certification: CRC certification is preferred but not required.

#M3

Ref: #558-Scientific

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Refine Your Search

protocol coordinator jobs

Clinical Research Coordinator III

Relief Referral Coordinator

Clinical Research Coordinator

Research Coordinator I, Patient Operations

Retail Onboarding Coordinator I

Clinical Research Coordinator

Infusion Coordinator Lead

Utilization Review Coordinator

Registered Nurse Care Coordinator

RN Care Coordinator

Therapy Coordinator

Registered Nurse - In-Patient Care Coordinator

Stability Coordinator I

RN Spine Coordinator, FT, Days, VUH

Cardiac Sonography Clinical Education Coordinator/Instructor

Board Certified Behavior Analyst-Clinical Coordinator

RN - Registered Nurse Coordinator - Transplant

RN - Registered Nurse Coordinator - Transplant

Assistant Athletic Trainer and Concussion Coordinator

Community Living Team Coordinator

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