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Clinical Research Coordinator III

Joulé

Carnegie, PA

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JOB DETAILS
SKILLS
Clinical Research, Communication Skills, Data Collection, Data Entry, Feasibility Analysis, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Interviewing Skills, Order Supplies, Organizational Skills, Protocol Analysis, Regulatory Compliance, Research Skills, Staff Training, Training/Teaching
LOCATION
Carnegie, PA
POSTED
6 days ago
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


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/