Clinical Research Coordinator III - GI Motility
About The Position
The GI Motility team is seeking a full-time Clinical Research Coordinator III who will join a highly collaborative and productive team focused on conducting a variety of research projects to understand motility disorders, advancing the current treatments, and improving quality of life. The CHOP team is leading a multisite study on Body Surface Gastric Mapping where the clinical research coordinator III will be the lead coordinator in addition to being a team member on a variety of studies including a motility registry and biorepository. Under the supervision of the Principal Investigator and/or the clinical research administrative director, the coordinator III responsibilities include, but are not limited to, screening and recruiting of research participants, interfacing with clinical care and lab staff to schedule research visits, ensuring adherence to study protocols, preparing and submitting regulatory documentation to the Institutional Review Board, developing and maintaining accurate clinical study databases, collaborating with sub sites. The ideal candidate is an exceptional communicator with strong organizational and time‑management skills.
Requirements
- Bachelor's Degree Required
- At least four (4) years of clinical/research coordination experience Required
- Intermediate knowledge of IRB and human subject protection
- Basic proficiency in data management systems/tools
- Excellent verbal and written communications skills
- Excellent time management skills
- Solid analytical skills
- Ability to collaborate with stakeholders at all levels
Nice To Haves
- Master's Degree in a related field Preferred
- At least five (5) years of clinical/research coordination experience Preferred
Responsibilities
- Applies in depth knowledge of clinical research and independently coordinates the activities of 1 or more large-scale, complex multi-center / multi-institutional studies
- Provides oversight in the preparation, management and monitoring of study budgets
- Accountable for study oversight at one or more sites/institutions
- May be responsible for conducting monitoring activities at one or more sites/institutions
- Prepares study sites for internal/external regulatory audits (sponsor, FDA, NIH, etc)
- Facilitates and/or leads research/project team meetings
- Educates and mentors internal and external clinical staff, research teams and other coordinators; provides resources, and consulting on difficult protocols or projects
- Independent of the PI assesses and critiques protocol feasibility and provides recommendations
- May support 1 or more PI sponsored INDs or IDEs
- Liaises between Research billing (CTFM) and the research team
- Participate in the informed consent process of study subjects
- Scheduling, facilitating and/or leading research/project team meetings
- Screen, recruit and enroll patients/research participants
- Report adverse events
- Comply with Institutional policies, standard operating procedures (SOPs) and guidelines
- Must comply with federal, state, and sponsor policies
Benefits
- Annual influenza vaccine
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
