Regional Clinical Research Associate, Vaccines vacancy at ReSearch Pharmaceutical Services in Northern

ReSearch Pharmaceutical Services is at the momment seeking for Regional Clinical Research Associate, Vaccines on Wed, 27 Mar 2013 16:43:32 GMT. The Regional Clinical Research Associate completes project activities associated with monitoring functions of Phase I-IV clinical research studies. The RCRA will perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs). Responsibilities include (but are not limited to) : Performs study start-up activities...

Regional Clinical Research Associate, Vaccines

Location: Northern New Jersey

Description: ReSearch Pharmaceutical Services is at the momment seeking for Regional Clinical Research Associate, Vaccines right now, this vacancy will be placed in New Jersey. For complete informations about this vacancy opportunity please give attention to these descriptions. The Regional Clinical Research Associate completes project activities associated with monitoring functions! of Phase I-IV clinical research studies. The RCRA will perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs).

Responsibilities include (but are not limited to) :
Performs study start-up activities related to monitoring activities.

Develops and implements innovative approaches for and participates in site recruitment, selection, and initiation activities.

Participates in CRA protocol specific training and development activities.

Develops and implements innovative approaches for the preparation and coordination of investigator meetings and participates in meeting.

Conducts site initiation visits with study site staff (train site personnel in GCP and study conduct)

Develops patient enrollment strategies with the project team and clinical trial sites.

Ensures the integrity of clinical data and adherence to applicable ! regulatory, protocol, and company guidelines.

Ensures! proper storage, dispensation and accountability of clinical trial materials.

Conducts interim monitoring visits (conducts source document verification of CRF against medical records).

Performs site management activities.

Conducts in-house monitoring activities as appropriate.

Review investigator regulatory files to ensure they are accurately maintained.

Maintains patient tracking records for assigned sites.

Conducts study site close-out visits.

Completes administrative activities as a member of the project team.

Qualifications :
Knowledge, Skills, and Abilities:
Excellent verbal and written communication skills

Excellent organizational, record retention, and time management skills

Excellent decision making skills

Excellent customer service and interpersonal skills

Knowledge of FDA regulatory requirements (i.e. GCPs, CFRs, etc.)

Passion ! for customer service

Education and Work Experience:
Bachelor’s Degree in allied health fields such as Nursing, Pharmacy, or Health Science, preferably with clinical trial monitoring experience; or RN with Associates Degree or 3 year Nursing Diploma with 2 years of clinical nursing experience

Minimum of 2-3 years of clinical research monitoring experience
- .
If you were eligible to this vacancy, please email us your resume, with salary requirements and a resume to ReSearch Pharmaceutical Services.

If you interested on this vacancy just click on the Apply button, you will be redirected to the official website

This vacancy starts available on: Wed, 27 Mar 2013 16:43:32 GMT



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