Clinical Research Scientist in Summit, NJ at Pyramid Consulting, Inc

Date Posted: 7/5/2020

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Summit, NJ
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:
    7/5/2020

Job Description

Immediate need for a talented Clinical Research Scientist with experience in the Pharmaceuticals Industry. This is a 6+ Months Contract opportunity with long-term potential and is located in Summit, NJ. Please review the job description below.
 
Job ID: 20-16689

Key Requirements and Technology Experience:
  • Review of clinical data within eCRF system, patient profiles, etc. to issue queries and clean data from clinical perspective
  • Conduct review of ongoing summary data including: safety, primary efficacy variables, and laboratory data.
  • Assist the Clinical Research Physician to interface with project team members including: Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management.
  • Prepare or assist with preparation of key documents e.g. Investigator Brochures, regulatory submission documents, internal or external presentations, etc.
  • Protocol preparation (writing, reviewing, amending and cross-functional facilitation as appropriate).
  • Clinical study report preparation
  • Review literature and prepare summary documents for inclusion in IB, protocols regulatory submission documents, etc.
  • Participate and/or Lead team meetings as required
  • Candidate must have experience working on clinical trials as a Clinical Research Scientist from a sponsor's perspective.
  • Must have at least two years of direct HEMATOLOGY/ONCOLOGY experience in a Clinical Research and Development, Clinical Science capacity
  • Must have experience performing data review in HEMATOLOGY/ONCOLOGY indications (note, this position is different in scope from a CRA position or clinical operations)
  • Experience in performing review of clinical trial data in order to identify trends in safety or efficacy data.
  • Ability to function independently in data review to identify discrepancies in clinical trial data and to write queries from a medical perspective.
  • Familiarity with Medidata, RAVE, J-review or other clinical databases or other data review tools (patient profiles, listings) would demonstrate the candidate's familiarity with the scope of work.
  • Some experience in medical writing such as authoring or co-authoring documents such as protocol, clinical study report, investigators brochure, patient narrative
  • Ability to communicate medical or clinical information to a physician.
  • Ability to understand clinical trial publications; understanding of disease
  • Degree in life sciences
Our client is a leading Pharmaceuticals Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. J2W:CB3