Clinical Research Coordinator III - GI Motility

SHIFT:
Day (United States of America)

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About the Job

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.

What you will do

• 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

Education

• Bachelor's Degree Required
• Master's Degree in a related field Preferred

Experience

• At least four (4) years of clinical/research coordination experience Required
• At least five (5) years of clinical/research coordination experience Preferred

Knowledge, Skills and Abilities

• 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

To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine. Learn more.
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SALARY RANGE:

$62,900.00 - $80,200.00 Annually

Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.

At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP's Compensation and Benefits.