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Bharathi Nekkanti's Jobs at DOCS
Recruiter | DOCS
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About Company
DOCS is the amalgamation of ICON Contracting Solutions and DOCS International, which together offer over 15 years of expertise in staffing the global pharmaceutical, biotechnology, clinical research and medical device industries.
Healthcare & Medical - NEW YORK, NY

Job Summary DOCS clients include small, mid and large sized Pharmaceutical companies in addition to many leading Biotechnology, Medical Device and CROs. As a global partner, DOCS currently offers global resourcing solutions to our clients. Roles & Responsibilities of the position Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team Acts as primary local company contact for assigned sites for specific trials. ...

View Site Manager-Oncology-NY/NJ Job - NEW YORK, NY
SITE MANAGER, CLINICAL RESEARCH ASSOCIATE,CRA,CMA,MONITORING ASSOCIATE
Research - NEW YORK, CA 100007

Summary: Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials. Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts. Principal Responsibilities: Responsible for analyzing contract requests/needs from operating companies and translating into appropriate contracts/budgets for company sponsored and investigator initiated clinical tr...

View Sr. Contracts and Grants Analyst Job - NEW YORK, CA 100007
Contracts Analysts, Contracts Specialists, Contracts Administrators, Contracts Negotiators, Contracts Managers
Research - CANADA , TN 00000

Job Title: Clinical Research Associate Experience: 3+ years Therapeutic areas:Oncology Location: Canada Roles & Responsibilities of the position PRINCIPAL RESPONSIBILITIES: - Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team - Acts as primary local company contact for assigned sites for specific trials. - Attends/participates in investigator meetings as needed. - Responsible for executing activities...

View Clinical Research Associate Job - CANADA , TN 00000
CRA,"clinical research associate",Oncology
Other - NEW YORK, NY

Job Summary DOCS clients include small, mid and large sized Pharmaceutical companies in addition to many leading Biotechnology, Medical Device companies and CROs. As a global partner, DOCS currently offers global resourcing solutions to our clients. Roles & Responsibilities of the position ESSENTIAL DUTIES AND RESPONSIBILITIES - Under the supervision of project lead or clinical study manager, help facilitate information flow between all members of the clinical operations/clinical trial site team, including in-house departments, clinical p...

View Clinical Research Associate Job - NEW YORK, NY
CRA,"clinical research associate"
Science & Biotech - Across USA, NY

Biostatistician or Statistician W2 or 1099 preferred 8+ years of experience working for a pharma or CRO No jumpers MS acceptable, PhD preferred - Plan and execute statistical contributions to Study Concept Documents, protocols, randomization specifications, Statistical Analysis Plans, Table, Figures, Listing shells, Submission Data File specifications, other key-study related documentation, protocol deviations, Clinical Study Reports and regulatory documents. - Independently support multiple studies/projects in different i...

View Biostatistician or Statistician Job - Across USA, NY
Biostatistician, Statistician,SOP,plan ,execute statistical, protocols analysis
Science & Biotech - Across USA, MA

Job Description Job Summary DOCS clients include small, mid and large sized Pharmaceutical companies in addition to many leading Biotechnology, Medical Device companies and CROs. As a global partner, DOCS currently offers global resourcing solutions to our clients. Roles & Responsibilities of the position W2 or 1099 preferred 5+ years of SAS experience working for a pharma or CRO CDISC experience (both SDTM and ADaM) BS acceptable, MS preferred Basic Qualifications: - BA/BSc or higher degree in Computer Science, Statistics, ...

View Statistical or SAS Programmer Job - Across USA, MA
SAS programming, CDISC ,SDTM ,ADaM,statistical programer