Must be commutable distance to Philadelphia, as you would need to be onsite 1-2 times a month for audits and/or staff meetings
Must live in one of the following states: PA, NJ or DE
-5-7 years of clinical research experience as a monitor/auditor, research nurse, research coordinator, regulatory affairs, quality control and assurance or compliance
-knowledge of human subjects clinical research
-strong understand of the principles of conducting compliance oversight
Additional Skills & Qualifications:
Must have a Nursing degree (RN/BSM) or BS in a scientific or related field
The appropriate candidate will possess a very strong working knowledge of federal regulations, GCP and IND/IDE in both adult and pediatric research. Must understand regulatory affairs and their applications to Quality Control and Quality Assurance; understand the application of federal, local and institutional regulations as they apply to the conduct of human subjects research.
Must be very comfortable working with MS Word and Excel, have very good understanding of medical records/patient charts organization and terminology; detail oriented; possesses excellent organizational and time management skills in a very diverse and fast-paced setting; have the ability to exercise discretion in working with highly confidential and sensitive data and subject matter; must be able to multi-task, prioritize and pivot to meet the demands of the department; must be able to work under pressure and exercise mature judgment, resourcefulness and initiative.
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
- Attention To Detail
- Clinical Research
- Clinical Research Coordination
- Human Subject Research
- Medical Records