Full-Time Research Assistant II

ESSENTIAL DUTIES AND RESPONSIBILITIES: Our employees are tasked with delivering excellent business results through the efforts of their teams. These results are achieved by:

• Assist with systematic and targeted literature reviews, indirect treatment comparison feasibility assessments, and landscape/gap assessments.
• Prepare research protocols, define and refine research questions related to literature review objectives, including protocols for registration (e.g., PROSPERO).
• Develop inclusion/exclusion criteria within the PICOS framework for screening.
• Screen abstracts and full-text articles (in DistillerSR and/or other tools) against defined criteria to assess suitability.
• Create PRISMA flow diagrams depicting study attrition.
• Perform article abstraction and validate data abstraction.
• Conduct study quality assessments/risk of bias assessments.
• Perform quality checks on various phases of the literature review.
• Develop draft publications (manuscripts, abstracts, posters) and reports.
• Lead and guide colleagues on literature reviews, feasibility assessments, and landscape assessments.
• Support training of peers and project setup on DistillerSR.
• Support development of best practices and standard operating procedures (SOPs).
• Participate in client meetings (attend teleconferences, record minutes).
• Perform all other duties as assigned.

Requirements:

• BSc or comparable degree in a medically-related field (e.g., biology, pharmacology, biochemistry, biology, or epidemiology).
• At least 1.5 years' experience in conducting systematic/structured literature reviews.
• Technical competency in EndNote and DistillerSR.
• Excellent written and verbal communication skills, with emphasis on synthesizing information.
• Strong analytical, problem-solving, and multitasking capabilities.
• Ability to adapt to shifting priorities, demands, and timelines.

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