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Jobs · Analyst · Pennsylvania

Clinical Research Coordinator II - Cellular Therapy and Transplant Section

Children's Hospital of Philadelphia · Philadelphia, PA · 1 wk ago
Analyst$58k–$73k/yrFull-time

Core responsibilities

  • Adhere to an IRB approved protocol
  • Participate in the informed consent process of study subjects
  • Support the safety of clinical research patients/research participants
  • Care for protocol related research procedures, study visits, and follow-up care
  • Screen, recruit and enroll patients/research participants
  • Maintain study source documents
  • Report adverse events
  • Understand good clinical practice (GCP) and regulatory compliance
  • Inform subjects and family on protocol, study intervention, etc.
  • Comply with Institutional policies, standard operating procedures (SOPs) and guidelines

Related responsibilities

  • Prepare, manage, submit, and maintain essential regulatory documents (e.g. IRB, FDA, etc.) and remain aware of the regulatory status for projects within scope of role
  • Register study on ClinicalTrial.gov as appropriate
  • Complete case report forms (paper & electronic data capture) and address queries
  • Facilitate pre-study, site qualification, study initiation, and monitoring visit as appropriate
  • Facilitate study close out activities as appropriate
  • Coordinate research/project team meetings
  • Organize and/or run study-related meetings locally or across teams (for multi-site projects)
  • Support study team communications and outreach
  • Provide training to junior staff on conduct of research studies
  • Document investigational product (drug/device) accountability
  • Self-monitor and self-audit responsibilities
  • Develop informed consent document and/or draft or edit IRB protocols or related documents such as study administration manuals
  • Develop Case Report Forms
  • Assignments to include more complex studies

Education Qualifications

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

Experience Qualifications

  • At least two (2) years of clinical/research coordination experience - Required
  • At least three (3) years of clinical/research coordination experience - Preferred

Skills And Abilities

  • Basic knowledge of IRB and human subject protection
  • Excellent verbal and written communications skills
  • Strong time management skills
  • Ability to collaborate with stakeholders at all levels

Benefits

The salary range for this position is $58,300.00 - $72,900.00 annually. Factors such as skills and experience could result in an offer above the salary range noted in this job posting.

Pay

SALARY RANGE: $58,300.00 - $72,900.00 Annually

Schedule

Full-time

Qualifications

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.

Benefits

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.

EEO / VEVRAA Federal Contractor

CHOP is an equal opportunity employer and is committed to creating a diverse and inclusive workplace. We celebrate diversity and are proud to be an EEO/AA employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law.

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