Senior Clinical Research Scientist (Oncology)

VersaTech Consulting Inc a division of Mascon Global a leader in the Information Technology Services Industry. With a reputation for quality service, VersaTech brings a long and successful track record of meeting the business needs of a wide range of Fortune 500 and middle market companies. These companies have come to expect ONLY THE BEST candidates from VersaTech and that’s exactly what we deliver. As a result VersaTech has established itself as the Primary Source of Contract and Permanent opportunities with our direct end clients in the Pharmaceutical/Biotech, Luxury Automotive, Manufacturing, Retail, Telecommunications and Financial/Banking industries.

We offer employment to W2 hourly, Independent Contractors and full time salaried employees. Our employees can take advantage of our competitive benefits package that includes a health plan, 401k, provisions for vacation and holiday pay, and technical and professional training. Compensation is commensurate with experience. VersaTech is an equal opportunity employer.

 

Minimum Education level Bachelor Degree Required

Senior Clinical Research Scientist (Oncology)

Location; Ridgefield Park, NJ

Fulltime Permanent Position

Our Direct Pharmaceutical End Client is looking for a Senior Clinical Research Scientist with Oncology experience to work in North New Jersey.

This is Fulltime Permanent position  

5 years of experience in clinical research in the pharmaceutical industry

Requires a Doctoral (Pharm D or Ph D) level degree (or Masters Degree)

Strong Oncology experience, budgeting & forecasting along with study design. Experience with Regulatory documents a must.

A thorough understanding of clinical research methodology including study design,

protocol writing and CRF preparation is required as is a knowledge of GCP and local regulatory requirements.

Working knowledge of the IND/NDA process acquired through direct industrial experience is required.

Knowledge of medical, scientific and clinical research techniques in assigned therapeutic area.

Preparing clinical trial Synopses and clinical trial Protocols. Prepares patient SAE narratives, section of the ISS, ISE, Investigator Brochure, etc.

Making recommendations for the supervision of monitoring, clinical trial conduct (enrollment, GCP practices, etc.).

Assisting in database evaluation / assessments.

Preparing drafts of clinical trial reports.

Assisting the Clinical Leader in the planning, implementation, managing, and reporting of clinical trials but may serve as Clinical Leader for selected trials.

5 years of experience in clinical research in the pharmaceutical industry

Requires a Doctoral (PharmD or PhD) level degree (or a Masters Degree)



Please respond with your word doc resume with availability / rate / contact details: dev.naik@mgl.com or dev.naik@vtcons.com or by Phone 732-726-4223

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