Syneos Health® is the only fully integrated end-to-end clinical and commercial solution organization. We are purpose-built for biopharmaceutical acceleration, creating better, smarter, faster ways to help clients navigate an increasingly complex marketplace. Our business addresses today’s market realities through clinical and commercial sharing expertise ...
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Works under minimal guidance and supervision of a line manager or delegate to assess the level of data required and approaches for RFPs and individual paid feasibility assessments.
Ability to manage and fulfill an average number of assignments concurrently. Requires little assistance with standard requests, is able to manage non-standard requests with guidance.
Assesses needs & independently liaises with internal stakeholders to review sponsor requirements, protocol, and timelines for individual RFPs.
Some contribution for development and achievement of departmental business objectives.
Liaises with Business Units, Business Development, Medical Directors, Business Analysts, and other members of the team to review sponsor requirements, protocol, and timelines for individual RFPs. Guided research of data assets and scientific literature using internet and internal facilities to provide background information. Includes query of relevant databases, including clinical trial registry tools and internal sources, and research various literature sources to support preparation of robust feasibility.
Maintains comprehensive records of work and stores all relevant data within internal libraries in a timely manner.
Provides review and assessment of the outcomes of pre-award site level outreach along with standalone feasibility assessments to inform on site selection, enrollment, and site activation activities.
Build and maintain relationships with internal and external stakeholders to develop clear communication methods to support study strategies with minimal adjustments
Qualifications
What we’re looking for
BS/BA in Science with an emphasis in medical research
Flexible, creative, and open to suggestions.
Self-motivated and ability to work both independently and as a critical part of a team.
Ability to understand and process scientific and clinical research documents.
Working independently, in a virtual team environment
Understanding and presenting complex scientific and clinical research data and analysis methodologies
Knowledge of principles, concepts, practices, and standards in the CRO industry
Effective text development
Working and managing individuals and data to drive business objectives.
Attention to detail
Advanced Microsoft Office Suite (e.g., Word, Excel, PowerPoint, database applications), email, and internet research capabilities.
Strong organizational, interpersonal, and team-oriented skills
Excellent verbal, editor-level written, communication proficiency.
Excellent time management skills; ability to perform several tasks simultaneously to meet deadlines in a dynamic environment
Ability to be flexible, adapt to change, as well as work collaboratively as part of a team
Must be flexible around travel and work hours if a business need should arise. Travel minimal less than 5%
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