Drug Safety Manager Pharmacovigilance

PAREXEL International - Billerica, MA

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END DATE April 05, 2012

Job Summary

Company
PAREXEL International... PAREXEL International
Location

Billerica, MA, US

Job Type
Regular
Job Classification
Full Time
Experience
not provided
Education
not provided
Company Ref #
300892300892
AJE Ref #
555610458
[+] More

Job Description

Drug Safety Manager Pharmacovigilance

Do you possess cutting edge drug safety pharmacovigilance experience & a thorough underst&ing of clinical trials? We are currently seeking recognized industry leaders to manage a team of drug safety associates, conduct training on processes & procedures, & represent the group to both internal & external clients. You will be challenged with assigning resources to new projects, assessing staffing needs for current & future projects, & ensuring that the work provided by the Drug Safety staff is in accordance with the hourly budget provided by Medical Business Operations. Additional responsibilities will include mentoring & training new staff, conducting annual appraisals of Drug Safety staff, & providing recommendations for promotions & career development.

GROWTH:
While most companies were busy downsizing, PAREXEL added over 2100 employees in 2009 alone!!

PROMOTION:
In 2009, more than 1200 PAREXEL employees received career promotions!!

EXPERTISE:
PAREXEL's experts, who have experience across a broad range of therapeutic areas, have supported nearly all of the top 50 best selling drugs that are on the market today.

AWARDS:
Scrip Award for Best CRO 2008, BioSingapore Award for Best Performing CRO 2009, Good Clinical Practice Journal, Most Innovative Patient Recruitment Strategy 2008,
Globe 100 - Top 10 Best-Performing Massachusetts-Based Public Company 2009 (including Top Employer Ranking by number of world wide employees)

Keywords: sae, adverse event, case processing, manager, nurse, rn, nursing, pharmacovigilance, drug, safety, clintrace, arisg, argus, oracle, aers, phase II, phase III, phase IV, EDC, electronic data capture, Rave, Inform, Datalabs, Impact, CTMS, ePRO, IVRS, IWRS, integration, clinical trial technology, eClinical, functional requirements, statistics, biostatistics, programming, sas, clinical, clinical research, phase IIIb, phase IV, phase IIIB/IV, project management, PM, project director, clinical trial, clinical trail, clinical study, CRO, pharmaceutical, biotechnology, biotech, medical device, oncology, clinical trials, clinical studies, project manager, implementation, client interaction, sponsor, pharma, biotech

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