July 30 2010
Senior Clinical Research Associate (Sr. CRA), USA, by Makro Scientific
View Makro Scientific profile and careers
Job description:
We at MAKRO deliver custom client-centric solutions by offering contract outsourcing and premium staffing to the most well known IT and Life Science Organizations throughout United States.
Our vision is to become a most reliable 'connector' between our clients and Talent pool i.e ' YOU '.
We have following opportunity currently available for you.
Job Title : Senior Clinical Research Associate (Sr. CRA)
Location : Bridgewater, NJ
Rate Range : Open
Description:
Prepares and reviews management reports, ad hoc reports, summaries, analyses on clinical databases. Coordinates and participates in co-monitoring of these investigations. Oversees the Quality Control review of clinical trial patient databases and clinical files. Prepares drug usage projections and tracking for assigned clinical investigations as requested. Participates in the periodic review and revision of departmental policies and SOPs to assure compliance with corporate policies, good clinical practice procedures (GCPs), or regulations of governmental agencies.
Contact:
I appreciate if you forward your updated resume, availability (if you are authorized to work in the United States for any employer), location and position preferences at ******** glenn.davis@makroscientific.com ******** for review before we speak.
OR
Contact our Recruitment Helpdesk at 973-679-5005.
Also if you have any friends or colleagues, working on similar skill set, kindly refer them as well as there are multiple open positions.
Thanks
Glenn
glenn.davis@makroscientific.com
Skills:
A minimum academic degree in Nursing (R.N. or B.S.N.), Life Sciences (B.A. or B.S.), Pharmacy or Medicine. Experience requirements may be less with advanced degrees.
An advanced degree (M.S. or PharmD) is preferred. 5-10 years experience of progressively increasing clinical research experience within the pharmaceutical industry, global experience a plus. Experience in drug development, especially FDA regulations and GCPs or Associates of Clinical Pharmacology CRA certification. Experience in IND/NDA/BLA submissions. Global experience or management of CROs a plus.
Ability to resolve and make judgements regarding administrative, scientific, and/or clinical problems with minimal supervision.
| Job Reference: | SCRA_JO_100309 |
| Job Category: | Pharmaceuticals Biotech Diagnotics [ View All Pharmaceuticals Biotech Diagnotics Jobs ] |
| Language requirements: |
|
| Employment type: | Full Time/Permanent |
| Salary: | open USD |
| Degree: | Bachelors |
| Experience (year): | 2 |
| Job Location: | Bridgewater, NJ USA |
| Address: | One Washington Park |
| Zip/Postal Code: | 07102 |
| Company Type | Recruiter |
| Post Date: | 03/10/2009 / Viewed 676 times |
Contact Information | |
| Company: | Makro Scientific |
| Contact Name: | Glenn |
| Contact Email: | glenn.davis@makroscientific.com |
| Contact Instructions: | I appreciate if you forward your updated resume, availability (if you are authorized to work in the United States for any employer), location and position preferences at ******** glenn.davis@makroscientific.com ******** for review before we speak. OR Contact our Recruitment Helpdesk at 973-679-5005. mention JobOutlets.com when applying for the position |
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