Clinical Research Nurse occupation at Axelon Services Corporation in New Haven

Axelon Services Corporation is currently interviewing Clinical Research Nurse on Sat, 06 Apr 2013 04:21:58 GMT. IS AN INITIAL SIX (6) MONTH ASSIGNMENT BUT DEFINITE POTENTIAL OF BEING EXTENDED FOR MORE THAN ONE YEAR BASED ON PERFORMANCE AND DEMAND. WORK SCHEDULE IS SHIFT WORK. Mostly 6am to 2:30pm M - F. ACTUAL JOB TITLE: CLINICAL RESEARCH NURSE. Position Purpose • Responsible for ensuring clinical trials are conducted in accordance with scientific, medical, and ethical principles, and within regulatory...

Clinical Research Nurse

Location: New Haven Connecticut

Description: Axelon Services Corporation is currently interviewing Clinical Research Nurse right now, this occupation will be placed in Connecticut. For complete informations about this occupation opportunity kindly read the description below. IS AN INITIAL SIX (6) MONTH ASSIGNMENT BUT DEFINITE POTENTIAL OF BEING EXTENDED FOR MORE THAN ONE YEAR BASED ON PERFORMANCE AND DEMAND. WORK SCHEDULE IS SHIFT WOR! K. Mostly 6am to 2:30pm M - F.

ACTUAL JOB TITLE: CLINICAL RESEARCH NURSE.

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.

• Organizational Relationships: • Reports to Lead./Supervisor of Research Techs and Nurses and/or Director of Operations Resources Managed (budget and FTEs): • Determine the necessary materials required for ! study conduct, as appropriate 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 - Assist in responding to & resolving! 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 & measurements) & those study activities requiring emergency nursing intervention - Serve as a lead nurse on a protocol, as appropriate - Review and provide input, to designated clinic team contact, on assigned synopses, protocols, and ICDs as available.

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 2 years 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 e! asily understandable language complicated research principles. - Must h! ave 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. • Highly Desirable: Drug development or phase 1 experience. Prior Experience Preferred • Minimum of 2 years general medical-surgical nursing experience including competency in phlebotomy techniques and performing electrocardiograms.

Technical and Behavioral Competencies: Competency Detail / Comments (specific skills, etc.) • Team Work • Clinical Skills • Support WWCROPs • Effective Communication • Flexibility • Computer Skills • Group members are able to perform and collaborate in teams to problem solve for increased team productivity. Emergency interventions are appropriate, immediate, and demonstrate excellent assessment skills and standard of care. • Successful study conduct of all Clinical Researc! h Unit studies in accordance with ethical, legal, and moral standards, Good Clinical Practices (GCPs) and Good Laboratory Practices (GLPs), Clinical Sciences and Clinical Research Unit management requests, and PGRD drug development goals. • Contribute to the business needs of WWCROP’s through the fulfillment of the essential functions specified in this role. • Demonstrates effective communication with management group and external customers. • Demonstrate ability and flexibility to work alternative or additional hours (weekends/evenings/nights) to provide study activity coverage. • Working knowledge of computers and clinical research data systems and associated issues/risks.

MUST HAVE 3-5 YEARS RELATED EXPERIENCE.

MOST CRITICAL: The research nurse must be ACLS certified, have good nursing skills, able to do ECG’s, vital signs,learn other procedures, assess subjects for adverse events, administer study medication. Willing to work in a cli! nic (ie Hospital setting).

There may be times when the nurse m! ay need to escort a subject to a local physician’s office or hospital (please have this built in to the bill rate if necessary as this will not be expensible).

REQUIRED PERSONALITY TRAITS: Professionalism, able to take direction, positive attitude, quick learner.

IS AN INITIAL SIX (6) MONTH ASSIGNMENT BUT DEFINITE POTENTIAL OF BEING EXTENDED FOR MORE THAN ONE YEAR BASED ON PERFORMANCE AND DEMAND. WORK SCHEDULE IS SHIFT WORK. Mostly 6am to 2:30pm M - F.

OVERTIME WILL BE NEEDED AT TIMES.

***WILL NEED TO BE CPR CERTIFIED PRIOR TO START.
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If you were eligible to this occupation, please email us your resume, with salary requirements and a resume to Axelon Services Corporation.

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This occupation starts available on: Sat, 06 Apr 2013 04:21:58 GMT

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