Senior Associate, Clinical Scientist I - Oncology

Employer
AbbVie
Location
Lake County, Illinois, USA
Posted
May 08, 2018
Ref
1801219
Required Education
Bachelors Degree
Position Type
Full time
Prepares scientific reports and presentations related to clinical trials using available software and templates. Reviews clinical protocols. Brings together all necessary data and information to prepare internal documents or scientific reports related to clinical trials; keep multiple reports moving forward simultaneously (multi-tasking). Key Responsibilities
  • Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
  • Coordinates advisory meeting agendas, activities and slide decks and consulting agreements
  • Complies with procedures set forth in:
  • Relevant IQS documents
  • Study protocols
  • Other directives issued by the management regarding clinical/ preclinical studies.
  • Independently applies experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded efficacy and safety reviews. Ensures scientific integrity of all processes
  • Applies the most current electronic document conventions and processes consistently and accurately.
  • Integrates clinical trial data across studies and identifies/resolves issues impacting projects. Provides this information to internal peers and therapeutic area management
  • Committed to producing work of the highest quality
  • Performs literature and competitive intelligence searches
Position Accountability / Scope
  • Receives assignments from Therapeutic Area MD or Scientific Staff and is responsible for completing clinical study objectives on schedule and largely unsupervised with consultation.
  • Uses resources appropriately and effectively to complete tasks and meet required timelines
  • Maximizes individual, therapeutic area and team productivity
  • Reviews key decisions impacting project timelines with management.
  • May mentor therapeutic area personnel
  • Minimum Experience / Training Required
  • Bachelors/Master's degree, in Science related to Field +8 years' experience in the pharmaceutical industry or PharmD/PhD/MD preferred
  • Understanding of clinical study principles
  • Possesses good oral and written communication skills
  • Proficient in using computer to analyze clinical study data, generate reports and create presentations, posters and manuscripts
  • Knowledge of complex scientific analyses, business-related procedures, and project leadership.
  • Experience supporting clinical research, drug development and/or therapeutic area operations.
  • Proven record of successful projects.
Basic:
  • Bachelors/Master's degree, in Science related to Field +8 years' experience in the pharmaceutical industry or PharmD/PhD/MD preferred
  • Understanding of clinical study principles
  • Possesses good oral and written communication skills
  • Proficient in using computer to analyze clinical study data, generate reports and create presentations, posters and manuscripts
  • Knowledge of complex scientific analyses, business-related procedures, and project leadership.
  • Experience supporting clinical research, drug development and/or therapeutic area operations.
  • Proven record of successful projects.

Equal Opportunity Employer Minorities/Women/Veterans/Disabled