Regional Clinical Research Associate, Multi-Therapeutic occupation at ReSearch Pharmaceutical Services in Dallas

ReSearch Pharmaceutical Services is presently looking of Regional Clinical Research Associate, Multi-Therapeutic on Tue, 15 Oct 2013 22:09:02 GMT. The Regional Clinical Research Associate completes project activities associated with monitoring functions of Phase I-IV clinical research studies. 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...

Regional Clinical Research Associate, Multi-Therapeutic

Location: Dallas Texas

Description: ReSearch Pharmaceutical Services is presently looking of Regional Clinical Research Associate, Multi-Therapeutic right now, this occupation will be placed in Texas. Further informations about this occupation opportunity kindly read the description below. The Regional Clinical Research Associate completes project activities associated with monitoring functions of Phase! I-IV clinical research studies. 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 stora! ge, 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 custo! mer 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

Minimum of 2-3 years of clinical research monitoring experience

Must be able to handle a workload of multiple protocols / multiple sites
- .
If you were eligible to this occupation, please email us your resume, with salary requirements and a resume to ReSearch Pharmaceutical Services.

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

This occupation starts available on: Tue, 15 Oct 2013 22:09:02 GMT

Apply Regional Clinical Research Associate, Multi-Therapeutic Here