About the Company
Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation headquartered in New York City. We are one of the world’s largest pharmaceutical companies, engaged in the discovery, development, manufacturing, marketing, and sale of healthcare products, including medicines and vaccines. At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives.
Job Description
We are seeking a dedicated and experienced Research Nurse with a strong focus on Clinical Trials to join our dynamic team in Rapid City, South Dakota. In this pivotal role, you will be instrumental in the execution and management of clinical research studies, ensuring patient safety, data integrity, and adherence to protocols. You will work closely with investigators, study coordinators, and other healthcare professionals to advance medical science and bring innovative treatments to patients. This position offers a unique opportunity to contribute directly to groundbreaking pharmaceutical research within a world-leading company.
Key Responsibilities
- Recruit, screen, and enroll eligible participants into clinical trials according to study protocols.
- Perform clinical assessments, vital signs, physical exams, and collect biological samples as per protocol requirements.
- Administer investigational products and medications safely and accurately.
- Monitor participants for adverse events, document findings, and report to investigators and sponsors.
- Educate participants and their families about the clinical trial, informed consent process, and study procedures.
- Maintain accurate and comprehensive study documentation, including source documents, case report forms (CRFs), and electronic data capture (EDC) systems.
- Ensure strict adherence to Good Clinical Practice (GCP) guidelines, IRB regulations, and all applicable federal and local regulations.
- Collaborate with the research team to schedule participant visits, manage study supplies, and resolve data queries.
- Assist with data analysis and preparation of study reports as needed.
- Participate in site monitoring visits and audits from sponsors or regulatory agencies.
Required Skills
- Active Registered Nurse (RN) license in South Dakota
- Minimum of 3 years of clinical nursing experience
- Strong understanding of medical terminology, disease processes, and pharmacology
- Excellent communication and interpersonal skills
- Proficiency in basic computer applications (Microsoft Office Suite)
- Demonstrated ability to work independently and as part of a multidisciplinary team
- Exceptional organizational skills and attention to detail
- Ability to prioritize tasks and manage multiple responsibilities effectively
Preferred Qualifications
- Bachelor of Science in Nursing (BSN)
- Prior experience in clinical research or clinical trials
- Certification as a Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP)
- Experience with Electronic Data Capture (EDC) systems
Perks & Benefits
- Comprehensive health, dental, and vision insurance
- Generous paid time off and holidays
- 401(k) retirement plan with company match
- Life and disability insurance
- Tuition reimbursement and continuing education opportunities
- Employee assistance program
- Wellness programs and resources
- Opportunity for professional growth and career advancement within a global organization
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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