Clinical Research Nursing Provider
il y a 4 semaines
ROLE SUMMARY
ROLE RESPONSIBILITIES
- Executes clinical research studies in accordance with scientific, medical, and ethical principles, within regulatory requirements/guidelines, and Pfizer SOPs
- Executes and is responsible for protocol required data and sample collection in accordance with ALCOA standards from screening until last final visit.
- Responsible for volunteer/patient safety including code carts and clinical supplies maintenance and readiness
- Observes and communicates to the medical provider, records, and updates any adverse event. Provides patient care within scope of licensure as needed under the supervision of medical provider.
- Responsible for self-daily check on data collected during study activities
- Maintains proficiency in multiple methods and forms of data collection (i.e., ECGs, V/S, venipuncture, telemetry, etc.).
- Provides instructions and assistance to clinical research participants.
- Assists in human biological sample management including generation of identifying labels, collection and associated source document completion as needed
- Maintains equipment log & calibration records as needed
- Maintains adequate levels of clinical supplies for data collection, clinical care and emergency readiness.
- At discretion of Clinical Services Manager, functions as an asset owner to keep equipment in functioning order through preventative maintenance and calibration
- Reports and documents any issue/incident/discrepancies in the conduct of a study
- Answers and resolves any query sent by project manager or clinical coordinator
BASIC QUALIFICATIONS
Minimum of a bachelor’s degree in Nursing or equivalent “Life Science/Biomedical” or “Health Care” related education or experience.
Current BLS/ILS/ACLS certification
Current Healthcare licensure as applicable per state/country statute.
Minimum of 2 years of relevant work experience in a health-related discipline including competency in phlebotomy/venipuncture techniques, and performing electrocardiograms is highly preferred.
Experience in pharmaceutical or medical research position is an asset
PREFERRED QUALIFICATIONS
Technical skills:
- Nursing and emergency interventions are appropriate, immediate, and demonstrate excellent assessment skills and standard of care
Computer skills:
- Working knowledge of computers (e-HR) and laboratory data handling acquisition systems and associated issues/risks.
- Proficiency in Microsoft (MS) Office and the ability to learn different software programs.- Scientific/ Clinical/ Research Knowledge:
- Understanding and comprehension of scientific writing- Language skills:
- Good written and verbal skills in French and Dutch are essential (BrusselsCRU only)
- Good written and verbal skills in English are essential (Brussels CRU only)
- Bilingual ability to speak, read, and write Spanish is highly desirable. (New Haven CRU only)- Communication:
- Excellent verbal and written communication skills- Other:
- Able to work effectively in multifunctional, interdepartmental management teams.
- Change agile: open and receptive, flexible and adaptable Business oriented
- Action-oriented: achieve departmental goals- Customer focus:
PHYSICAL/MENTAL REQUIREMENTS
Physical effort: duties involve light effort. Work involves up to 5 pounds/2,5kg of force to lift, carry, push, pull or move objects.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Required to work on shift (week-end/legal holidays/evening/night)
Might be required to work on unsocial hours or overtime to guarantee study execution business continuity.
Might be required to do some intercontinental travels between PCRU and research sites.
Reports to Clinical Services Manager
Functional working relationship with Project Managers, Technical Training Manager, Clinical Coordinators, Systems Administrator, Quality & Compliance Managers and Laboratory Staff.
Functional working relationship with PCRU Medical Provider staff in areas of medical oversight and intervention
- Pfizer discovers, develops, manufactures and distributes medicines and vaccines. Pfizer wants to contribute to better health and wellness for everyone, at every stage of life. Pfizer works with the government and other health partners to provide quality and accessible healthcare. The patient is central to this story._
- Pfizer has four offices in Belgium with which it supports its Belgian and international activities: 1) Anderlecht, where the Pfizer Clinical Research Unit is located. This is a fully equipped phase 1 research center. With that of New Haven (US), it is one of two Phase 1 Pfizer research centers in the world, 2)_
- _
- Elsene_
- , the Belgian headquarters, 3)_
- _
- Puurs_
- , Pfizer's production and packaging site, and 4) Zaventem, the international Pfizer's Logistics Center._
- More information can be found at_
- _- ,_
- _- _
- and on Facebook and Twitter._
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