Clinical Trial Project Manager - SAE, Pharmacovigilance or Eudravigilance

$144,000

Closed
Starts on 12/17/18
Occasional travel to Philadelphia, PA  
Daily Rate
$1,100/day
Duration
6 mo.
Intensity
40 hr/week

About The Work

Interim Support & Leadership
Project Manager
*50% onsite in historic Philadelphia, PA and 50% remote.*
*Full time for 6-12 months*

We need strong clinical project managers for two opportunities.

Opportunity 1: A pharma company is trying to create uniform clinical standards. The goal is to drive the implementation of a common SAE (Serious Adverse Events) across multiple pharmaceutical companies for clinical trials.

Opportunity 2: You'll manage a project to implement best processes and procedures in the pharmacovigilance area within the Clinical Trial space. Candidates MUST have pharmacovigilance and eudravigilance experience.

Both assignments are full-time and will last 6-12 months. East Coast candidates are preferred, but others are welcome to apply.

Sectors

Healthcare
Biotech

Prerequisites

5-10 years professional experience
Ideal Candidate
Applicants MUST have clinical pharmaceutical experience. This is an opportunity for you to quarterback a big, cross functional project.
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