Clinical Research Manager

Jefferson Health System

$80K — $110K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s Degree required; Master's Degree preferred
  • 5 years of clinical research experience with Bachelor's; 3 years with Master's
  • 2+ years of project management experience
  • Strong knowledge of regulatory agency processes
  • Experience with developing and updating standard operating procedures (SOPs)

Responsibilities

  • Manage multi-site trials, ensuring effective document management and IRB tracking
  • Direct preparation and submission of regulatory applications and correspondence
  • Supervise research staff, including training and performance evaluations
  • Ensure compliance with domestic and international regulations
  • Identify issues and recommend changes to enhance regulatory compliance

Benefits

  • Comprehensive medical, dental, and vision insurance
  • Life and AD&D insurance, short- and long-term disability
  • Flexible spending accounts and retirement plans
  • Tuition assistance and discounts after service period
  • Access to voluntary benefits with group rates and discounts
Full Job Description

Job Details

The Clinical Research Coordinator IV trains research staff, supervises staff and oversees clinical trials from start-up to close-out. Develops and/or contributes to standard operating procedures and processes. Attends and engages in leadership meetings, represents TJU internally and externally, and oversees research operation in department, and provides expert consulting at an institutional level.

Job Description

  • Manages all Investigator-lead multi-site trials by developing and implementing processes for document management and IRB submission tracking (i.e. continuing reviews and amendments) for multi-center trials as well as have protocol status knowledge.
  • Directs the preparation and submission of regulatory agency applications, reports, and correspondence for opening new studies, protocol amendments, informed consents, continuing reviews, FDA safety reporting, Investigational New Drug applications (INDs), annual reports, Investigational Device Exemption applications (IDEs), etc.
  • Provides direct supervision of the research staff which includes conducting on-going training, reviewing workloads, completing annual evaluations, etc.
  • Oversees documentation efforts to ensure compliance with domestic and international regulations and standards.
  • Identifies issues, recommends changes, writes new standard operating procedures (SOPs) or update existing SOPs with the goal of enhancing regulatory compliance.

Education:

Bachelor’s Degree Required

AND

Experience:

Bachelors Degree and 5 years of clinical research experience or Master’s Degree and 3 year clinical research experience. 2+ years of lead/Project Management experience.

Work Shift

Workday Day (United States of America)

Worker Sub Type

Regular

Employee Entity

Thomas Jefferson University

Primary Location Address

1015 Walnut Street, Philadelphia, Pennsylvania, United States of America

Benefits

Jefferson offers a comprehensive package of benefits for full-time and part-time colleagues, including medical (including prescription), supplemental insurance, dental, vision, life and AD&D insurance, short- and long-term disability, flexible spending accounts, retirement plans, tuition assistance, as well as voluntary benefits, which provide colleagues with access to group rates on insurance and discounts. Colleagues have access to tuition discounts at Thomas Jefferson University after one year of full time service or two years of part time service. All colleagues, including those who work less than part-time (including per diem colleagues, adjunct faculty, and Jeff Temps), have access to medical (including prescription) insurance.

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