Urgent requirement for one of our top clients located in “Mountain View, CA ”.
Please contact me at your earliest convenience, along with job No. SCRA_113007 to xxxxxx.xxxxxx@xxxxxxxxx.xxx
Description:
Monitor clinical trials, study sites, and clinical data. Ensure compliance with protocol and overall clinical objectives and GCP. Provide project support to clinical programs with minimum supervision. Interfaces with all project/clinical groups and off-site personnel as needed in support of project and departmental goals and responsibilities. Manage clinical study sites including study site start up and close-out. Ensure study sites follow Company’s SOPs and GCP. Assist in management of relationships with vendors within and across studies. Provide mentoring and work leadership to junior CRAs.
Assist in development of clinical study protocols and take ownership of their implementation where appropriate. Monitoring of clinical study sites (CRO staff) as required Ensures identified clinical study issues are resolved; implements and monitors corrective action. Provide input into development of Case Report Forms.
Requirements
Bachelor's degree or equivalent. RN with evidence of further study considered. Major course of study in Science or Health-related preferred. Training & Experience: 5 years experience in Clinical Research or related field. MUST be proficient in Microsoft Office/Windows, and Microsoft Outlook. Specifically: MS Word, MS Excel, MS Powerpoint and MS Project with excellent oral and written communication skills. Demonstrates good understanding of ICH/GCP, and US FDA regulations as applied to clinical research.
Contact:
The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) to *** xxxxxx.xxxxxx@xxxxxxxxx.xxx ***
Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us.
|
