Drug Safety Professionals - Highest Pay

Drug Safety Professionals  - Highest Pay

 

We are in need of several highly qualified pharma clinical and drug safety professionals. Must have good skills in communication, managing multiple priorities and computer literacy. We are looking for experienced:

 Drug Safety AssociatesDrug Safety ScientistsClinical Research AssociatesClinical Data ManagersClinical Coders

 

The ideal candidates should have experience in drug safety, clinical trial data management, or adverse event reporting. Must have advanced understanding of pharmaceutical clinical trial methodology, GCP and medical terminology. Understanding of dictionary philosophy specifically with regard to MedDRA and WHODRA. Good understanding of physiology, pharmacology, clinical study objectives and the drug development process. 

 

CRAs will participate in site nomination processes; perform evaluation of site capability to deliver the contractually agreed to number of patients, ensure high quality data, and make recommendations for inclusion in clinical trials.  Experience with ClinAdmin.

 

Data managers will be Responsible for providing timely and professional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be declared clean and locked according to strict performance standards. Review and contribute to the development of trial validation plan related documents and create/approve final CRF design, validation checks and reports necessary to assure high quality and consistent data.

 

*** Highest compensation and benefits in the industry.   ***

 

We are looking for either contract consultants or FT employees.

 

Locations:

Parsippany, NJ

 

This is a great opportunity to work in an exciting professional environment, while gaining superb experience, with tremendous growth potential.

 

If you are interested, please email a formatted copy of your resume to nicole@ivorysystems.com

 

 

Principles only, no third parties please.

 

 

/EOE