Responsibilities will include, but are not limited to, the following: • Degree in Life Sciences (e.g., nursing, pharmacy, biology or related medical field) • Oncology or hematologic oncology experience • Experience in clinical research & development or equivalent; at least one year in a CR&D capacity performing data review in oncology/hematology • Experience working on clinical trials from a Sponsor’s perspective • Experience in performing review of clinical trial data in order to identify trends in safety or efficacy data; identifying • Ability to identify discrepancies in clinical trial data and to write queries from a medical perspective. Familiarity with INFORM, 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 understand clinical trial publications; understanding of disease • Support other clinical trial activities as requested • This position is different in scope from a CRA or laboratory scientist position • Excellent written and verbal communication skills and interpersonal skills. • Demonstrated ability to work as part of a team. EducationMinimum of a Bachelor’s/Master's Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.