At a Glance
- Tasks: Coordinate clinical trials and ensure regulatory compliance in a dynamic medical environment.
- Company: Join Temple University's Lewis Katz School of Medicine, a leader in medical research.
- Benefits: Enjoy full medical coverage, paid time off, tuition remission, and a generous retirement plan.
- Other info: Collaborative culture that values diversity and offers excellent career growth opportunities.
- Why this job: Make a real impact in healthcare while working with a diverse and innovative team.
- Qualifications: Bachelor’s degree and 3 years of experience in research or regulatory compliance required.
The predicted salary is between 50000 - 55000 £ per year.
Temple University's Lewis Katz School of Medicine's Pulm/Critical Care/SleepMed Department is searching for a Regulatory Program Coordinator to join our team.
Benefits:
- Full medical, dental, vision coverage
- Paid time off
- 11 Paid Holidays
- Tuition remission – eligible employees and their dependents can obtain a degree tuition free
- A generous retirement plan and so much more!
Salary Grade: T25. Salary Range: $50,000.00 - $55,000.00.
This role is also eligible for our employee referral program – TERP! Current employees can earn up to $500. Conditions apply. Please contact the HR Employment Office for details.
Job Details:
- This position will be on-site
- This position requires the following background checks: Cash Handling
- This is a grant funded position
Position Summary:
The Regulatory Program Coordinator, under the supervision of the Regulatory Manager, participates in the coordination of active Phase I-IV clinical trials and interacts with study sponsors, PI’s, and research clinical staff in the Lewis Katz School of Medicine’s Thoracic Medicine & Surgery department. At Temple, you will find it easy to fit in while staying true to yourself. We value what makes each employee unique and strive to maintain a culture of diversity and inclusion. As an employee, you will enjoy our collaborative team-based culture that values innovation and creativity.
Required Education and Experience:
Bachelor’s degree and at least three years of experience in research and/or regulatory compliance in a research or clinical setting. An equivalent combination of education and experience may be considered.
Responsibilities:
- Assist to maintain the oversight of all regulatory compliance monitoring including internal and external progress reports
- Prepare and process all regulatory documentation through the IRB including new submissions, continuing reviews, amendments, adverse events and reportable events
- Organize and maintain all regulatory affairs documentation/files
- Support compliance and quality assurance activities
- Participate in site visits, monitoring, audit and close‑out visits
- Participate in study team meetings, other required group meetings, and ongoing protocol training/compliance meetings
- Assist in the development of investigator‑initiated protocols, assist with IND applications and annual reports
- Assist with regulatory compliance guidance oversight of investigator‑initiated multi‑center trials
- Train research personnel on consent process/forms and the regulatory processes and regulatory documents.
- Perform other duties as assigned
Required Skills & Abilities:
- Demonstrated knowledge and understanding of complex federal regulations, ethical issues, institutional policies, and other federal agency requirements governing human subjects research.
- Demonstrated knowledge of quality assurance or auditing functions.
- Demonstrated computer skills, and proficiency with MS Word, MS PowerPoint, MS Access or similar software programs.
- Excellent interpersonal and customer service skills, along with the ability to effectively collaborate with a diverse constituent population.
- Excellent verbal and written communication skills, including training skills.
- Demonstrated organizational and time management skills, along with the ability to work under tight deadlines.
- Demonstrated ability to be detail‑oriented.
- Demonstrated ability to work independently and as part of a team.
- Must maintain a working knowledge of current regulations, guidelines, and trends influencing the conduct of human subjects research.
- Ability to travel to off-site locations that may not be accessible via public transportation.
Preferred:
- Experience with biomedical human research is preferred.
Diversity Statement:
Temple University values diversity and is committed to equal opportunity for all persons regardless of age, color, disability, ethnicity, marital status, national origin, race, religion, sex, sexual orientation, veteran status, or any other status protected by law.
Compliance Statement:
In the performance of their functions as detailed in the position description, employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution. Employees are also expected to understand and be in compliance with applicable laws, University and employment policies and regulations, including NCAA regulations for areas and departments which their essential functions cause them to interact.
You may request a copy of the report by calling Temple University's Department of Public Safety at 215‑204‑7900.
Regulatory Program Coordinator employer: Temple University
Temple University's Lewis Katz School of Medicine offers an exceptional work environment for the Regulatory Program Coordinator role, characterised by a strong commitment to diversity and inclusion. Employees benefit from comprehensive medical coverage, generous paid time off, and tuition remission for themselves and their dependents, fostering both personal and professional growth. The collaborative culture encourages innovation and creativity, making it an ideal place for those seeking meaningful and rewarding employment in the healthcare sector.