Clinical Research Coordinator Jobs

W2 Requirement, Onsite:
Harbor Clinical, a certified women owned clinical service firm is seeking a Clinical Study Coordinator located in the Philadelphia, PA area. The role is a contract position for 20 to 30 hours per week requiring onsite presence at the Children's Hospital of Philadelphia.


Responsibilities:
Supports research site with GCP compliance
Provides GCP training and SOP development services
Provides support on clinical research protocols.
Supports recruitment, scheduling, and patient screening
Support the management of day to day operations of clinical research studies
Follow participants in complex studies
Collect and maintain documentation of clinical research data
Experience with consenting, scheduling and checking the eligibility of patients
Hels site prepare for regulatory and initiation visits by monitoring safety reports, completing start up source documents, maintaining compliance documents, and assisting in protocol feasibility evaluation with Principal Investigator
Organizes the storage and use of the study related materials
Participates in the labeling, organization, storage and retrieval of study bio-specimens
Coordinates with laboratory for sample analysis.
Processes laboratory samples and deliver samples to laboratory
Monitors deadlines and prepares IRB applications, progress reports and informed consent forms
Monitors serious adverse events reports and prepares appropriate documentation for IRB and completes case reports forms.

Qualifications:
5+ years of experience as a clinical study coordinator
Strong GCP experience and leadership ability to train research sites
Experience in rare disease indication
SOP writing experience
Bachelor’s degree in Biological Sciences/Chemistry or related science is required
Experience facilitating trials for complex cases
Skilled in Microsoft Office Suite
Excellent interpersonal and organizational skills
Excellent communication skills
Team player with good ability to with other staff on project.