| Pfizer Inc. |
| Biotech and Pharmaceuticals |
| Existing work authorization required for United States |
| Direct Hire, Full-Time |
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****** |
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Throughout our 153 years, a legacy of caring for others has
been at the heart of everything we do at Pfizer. This
commitment is no less important when it comes to our
employees. Pfizer wants to ensure that employees have
resources to help them dev |
| Not specified |
Health - Research
Nursing - Other
|
| See below |
| from anywhere |
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See below
|
| See below |
| See below |
English
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| No cover letter requested |
| RUSAPFZ2182-604128 / Latpro-1760727 |
| Jul-01-2008 |
| Connecticut, Zip not provided |
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Description |
Description: Position Purpose
¢ Responsible for ensuring clinical trials are conducted in accordance with scientific, medical, and ethical principles, and within regulatory requirements/guidelines. Responsible for volunteer safety & accurate interpretation and execution of research protocols including multiple study activities such as: nursing assessments of physiologic response to drug administration; administration of study medication; cardiac monitoring; basic nursing care & emergency interventions, collection and electronic and/or written documentation of data. Assist in the design as it relates to feasibility, implementation, and reporting of clinical trials.
Primary Duties:
¢ The major duties and responsibilities will include but are not limited to:
- Safety monitoring of all study activity for assigned Protocol Document volunteer's activities while involved in assigned protocols
- Administer study medication in accordance with protocol
- Collaborate with study team to execute protocol.
- Monitor & document study subject compliance
- Record adverse events & update as appropriate
- Facilitate compliance of study subjects to protocol activities
- Maintain accuracy, accessibility, & confidentiality of volunteer records and reports
- Demonstration of communication skills & general behaviors which facilitate positive attitudes & trust in the volunteer populations toward participation in Clinic research
- Monitor & summarize clinical data by reviewing printouts & tables, looking for trends, interpreting abnormal lab parameters & adverse events, writing clinical summaries for clinical trials & maintenance of the formal Unit study file
- Receive, respond, & resolve all queries specific to subject data collection
- Maintain competency to assist with the execution of general technical activities (collection & processing of biological samples, vital sign & other physiological testing & measurements) & those study activities requiring emergency nursing interventionCompany Profile: Imagine a career that touches the lives of people everywhere. Imagine an oppurtunity to reach beyond your area of expertise to make an impact on something greater than the bottom line. Imagine playing a key role in some of the most critical issues facing healthcare today. This is your career at Pfizer - a career unlike any other.
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Requirements |
Training & Education Preferred:
¢ Bachelors Degree preferred
¢ Diploma or Associate's degree in Nursing, and/or Bachelor's degree (B.S./B.S.N) with valid CT nursing licensure.
- Minimum of 1 year general medical-surgical nursing experience including competency in phlebotomy techniques and performing electrocardiograms.
- Must have current ACLS certification.
- Clinical Research Experience preferred.
- Superior written and verbal skills are essential; including the ability to communicate in easily understandable language complicated research principles.
- Must have the ability to function as an effective team member in diverse workgroups to accomplish business objectives.
- Must have a working knowledge of computers, medical conditions, research techniques, and the application of clinical research.
Prior Experience Preferred
¢ Minimum of 1 year general medical-surgical nursing experience including competency in phlebotomy techniques and performing electrocardiograms.
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