Global Feasibility Specialist II
hace 2 días
Syneos Health Commercial Solutions is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do.
We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health Commercial Solutions easier to work with, but to make us easier to work for.
We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Salary: $80,000 - $110,000 per year
Job Responsibilities:
- Works under 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.
- Manages a limited number of project assignments of minimal to moderate complexity under supervision of a line manager or delegate.
- Responds to standard, routine requests in consultation with line manager or designee and applies data, knowledge/skills to outlined, known data collection activities.
- Under guidance and supervision of a line manager or delegate, liaises with internal stakeholders to review sponsor requirements, protocol, and timelines for individual RFPs.
- Limited and guided research of scientific literature using internet and internal data assets to provide background information. Query 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 as per outlined processes.
- Builid relationships with internal and external stakeholders to develop clear communication methods
Qualifications:
- BS/BA in Science with an emphasis in medical research
- Nominal experience in science or related field.
- Attentive to detail in the analysis and presentation of data.
- Flexible, creative, and open to suggestions.
- Self-motivated and ability to work both independently and as a critical part of a team.
- Working independently, in a virtual team environment
- Understanding and processing of scientific and clinical research data and analysis methodologies
- Knowledge of principles, concepts, practices, and standards in the CRO industry.
- Strong organizational, interpersonal, and team-oriented skills
- Excellent verbal, written, communication proficiency.
- Excellent time management skills; ability to perform several tasks simultaneously to meet deadlines in a dynamic environment
About Us:
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
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