Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Supportive policies and well-being initiatives tailored to support you and your family
- Commitment to a continuous learning culture with engaging work experiences
- Inclusive workplace free of discrimination and harassment
- Competitive total reward package including base pay and variable pay recognition programs

What to Expect (Job Responsibilities):
- Serve as a subject matter expert for nursing administration related to Investigational Product Preparation and Administration Instructions (IPPI)
- Co-author the IPPI and provide input on forms related to IP administration and dosing for clinical trials
- Develop training materials and conduct internal staff training on IP administration processes
- Assist in site assessments and provide recommendations for site/investigator selection in collaboration with the trial team
- Act as the point of contact for the internal study team regarding IP administration questions and issue resolution

What is Required (Qualifications):
- A degree in general nursing is required
- 3-4 years of recent clinical/hospital experience is required
- Minimum of 3 years’ experience with various IP administration routes (IV, SC, IM)
- Clinical trial research experience
- Strong written, oral, and interpersonal communication skills

How to Stand Out (Preferred Qualifications):
- Experience in antibody treatment, particularly in Oncology (hematology and solid tumor) and/or Immunology Therapeutic Areas
- Knowledge of the drug development process and International Council on Harmonization (ICH)/Good Clinical Practices (GCP)
- Innovative mindset with strong attention to detail
- Ability to collaborate across a matrix organization and manage multiple trials in parallel

#ClinicalResearch #Nursing #CareerOpportunity #ContinuousLearning #InclusiveWorkplace

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