Job Title: Senior Clinical Research Associate (SCRA)
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Vacancy details
Vacancy description:
Job Code:
00326
Job Title:
Senior Clinical Research Associate (SCRA)
Job Category:
Clinical Research
Contract:
Permanent
Discipline:
CRA, Clinical Study Coordinator
Country:
United States Of America
Location:
New Jersey
Min experience:
2 years
Annual salary:
Negotiable
Apply by:
05 Sep 2008
This is an excellent opportunity for a CRA with significant monitoring experience to work for an independent, pharmaceutical company that operates internationally, and focuses primarily on analgesics alongside oral contraceptives and treatment for respiratory tract disease. They are seeking a Clinical Research Associate at their US office in Bedminster, New Jersey to monitor the company's clinical studies.
JOB ROLE – Principal Tasks & Responsibilities include:
•The development of study specific documentation
•Monitoring and/or co-monitoring of the study.
•Recruitment tracking and supervising study sites.
•Training of study personnel at investigator's sites.
•Coordinating the approval process for the performance of clinical studies/notification to IRBs and authorities with regard to the respective study site.
•Tracking and assurance of data quality at the site.
•Site documentation at the investigator and in-house.
•The organization and performance of investigator meetings.
•Assisting with the site selection process.
•Assessing the suitability of facilities at study centre.
•Closing study and archiving documents.
•Contributing to other activities of the Study Team as defined in the respective team profile.
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
•Bachelor's degree or diploma in Nursing, Science or Medical, Medical/Technical, Pharmaceutical, Scientific or Laboratory training.
•Minimum of 2-3 years monitoring experience.
•Understanding of drug development process over different phases.
•Understanding of global regulations and guidelines.
•International and intercultural work experience is advantageous.
PERSONAL SKILLS & ATTRIBUTES:
•Organizational skills with attention to detail.
•Strong communication skills
•The ability to work in a team setting
•Any foreign language is an asset.
BENEFITS OF THE ROLE: This company boasts a supportive and friendly working environment with no red tape where the individual is given enormous latitude to formulate and express his/her own ideas. They have a vast array of on the job training courses and a management that promotes independent thinking among their employees. They offer competitive salaries plus an attractive compensation package with excellent benefits that include pension, healthcare and company bonus.
Fforde is a uniquely specialised recruitment agency/business for the pharmaceutical, clinical research and biotechnology sectors.
KEY WORDS: Senior Clinical Research Associate, SCRA, Clinical Monitoring, Monitor, Clinical Studies, Clinical Research, Clinical Trials, Clinical Study Data, Site Selection, Study Documentation, Archiving, Trial Master File, TMF, Nursing, Science, Medical, Medical/Technical, Pharmaceutical, Scientific, Laboratory, Drug Development, Global Regulations
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