Clinical Research Coordinator - Leukodystrophy Center

Children's Hospital of Philadelphia; Philadelphia (Philadelphia County); On-site; USD 60,000 - 80,000; Full time

Job summary

Children's Hospital of Philadelphia is seeking a Clinical Research Coordinator for the Leukodystrophy Center. This role involves independent coordination of clinical research activities, oversight of study budgets, and mentorship of clinical staff. Ideal candidates will have a Bachelor's degree and significant experience in clinical research coordination, with a strong commitment to advancing pediatric care.

Qualifications

• Bachelor's Degree required; Master's preferred.
• At least four years of clinical/research coordination experience required.
• Intermediate knowledge of IRB and human subject protection.

Responsibilities

• Coordinate activities of large-scale, complex multi-center studies.
• Prepare study sites for regulatory audits.
• Screen, recruit, and enroll patients/research participants.

Skills

Communication

Time Management

Analytical Skills

Collaboration

Education

Bachelor's Degree

Master's Degree in a related field

Tools

Data Management Systems

Job description

Clinical Research Coordinator - Leukodystrophy Center

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Clinical Research Coordinator - Leukodystrophy Center

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Seeking Breakthrough Makers

Children’s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation.

SHIFT:

Day (United States of America)

Seeking Breakthrough Makers

Children’s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation.

At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care—and your career.

CHOP does not discriminate on the basis of race, color, sex, national origin, religion, or any other legally protected categories in any employment, training, or vendor decisions or programs. CHOP recognizes the critical importance of a workforce rich in varied backgrounds and experiences and engages in ongoing efforts to achieve that through equally varied and non-discriminatory means.

About The Job

This role functions independentlyin a clinical research setting and is responsible for the complete coordination of assigned clinical research activities within the scope of clinical research protocols. May have supervisory responsibilities of study team staff.

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/projectteammeetings
• 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, professionals working onsite - at any CHOP location, for any portion of time - must be vaccinated for COVID-19. Learn more. EEO / VEVRAA Federal Contractor | Tobacco Statement

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care

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