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Online Resumes with "Regional CRA"
The RS-CRA will be directly responsible for conducting site qualification, initiation, interim monitoring and study closeout visits in accordance with all applicable regulations, guidelines, and business processes and will monitor the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas. Report monitoring activities and study site conduct via written reports. Interact and build...
To obtain a regional Clinical Research Associate position in the Philadelphia Area
To obtain a contract regional CRA position within the Midwest with an established device of pharmaceutical company. Willing to travel outide of the Midwest region.
Senior/ Lead Clinical Reseach Associate - over 15 years experience monitoring, site management, medical record review, training/mentoring junior CRAs. database locks. regional clinical team leader
My goal is to secure a regional, home-based position in which I can use my knowledge of all phases of clinical research to develop tools to collect data (CRFs/edit checks; to verify the data (site management/monitoring), clean data (database locks)and to insure patient safety by assuring all AE/SAEs are reported, protcols and infomed consent are IRBs approved and adherence to all ICH guidelines and regulations.
SUMMARY OF QUALIFICATIONS • Foreign graduate Medical Doctor and licensed RN with more than 22 years of clinical and research experience. US citizen. Fluent in English, Russian and Romanian • Extensive training in Good Clinical Practices, ICH Guidelines, SOPs through various Sponsors • In depth therapeutic and protocol knowledge as per Sponsor’s assignment. Excellent organizational and problem-solving skills.
Ideal Companies: Biotech companies
TO OBTAIN A SENIOR LEVEL REGIONAL CRA POSITION, HOME-BASED, WHEREBY MY 12 YEARS OF MONITORING CLINICAL TRIALS MAY BE UTILIZED.
Tags for this Online Resume: Regional Clinical Research Associate