Description
Global Feasibility Specialist | Ideal Opportunity for Study Coordinators (Oncology desirable) | Hybrid | Buenos Aires, Argentina
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
Job Summary
Responds to standard feasibility requests of limited complexity in a timely manner within the Global Feasibility Process to meet the business objective timelines of the proposal deliverable, under supervision of a mentor or line manager. Coordinates the collection and analysis of data to support the development of country and site strategies for proposal and independent project feasibility assessments.
Provides additional informatics and data intelligence around patient access and country suitability, competitive environment, enrollment analysis, and supportive enrollment modelling. Attends strategy calls and liaises with Business Unit representatives, Medical Directors, Proposal Analysts, and Business Development to review sponsor requirements and protocols for Requests for Proposals (RFPs) and Requests for Information (RFIs).
Prioritizes and organizes own work to meet agreed upon deadlines.
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
- Build 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.
- Sales or other text development
- Working with individuals and data to drive business objectives.
- Attention to detail
- Microsoft Office Suite (e.g., Word, Excel, PowerPoint, database applications), email, and internet research capabilities.
- 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
- 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 typically less than 5%
Get to know Syneos Health
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.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Provides Global Feasibility business deliverables while working independently with minimal oversight across all indications. Plans, prioritizes, organizes, and completes work effectively to meet established objectives. Responsible for research and analysis of data to support the development of country and site strategies for proposal and independent project feasibility assessments, as well as troubleshooting project issues. Provides advanced critical thinking and application of informatics and intelligence around patient access and country suitability, competitive environment, enrollment analysis, and supportive enrollment modelling. Attends strategy calls and liaises with Business Unit representatives, Medical Directors, Proposal Analysts, and Business Development to review sponsor requirements and protocols for Requests for Proposals (RFPs) and Requests for Information (RFIs). May mentor a team of Feasibility specialists in the collection and analysis of feasibility data, provision review and editing of feasibility text/reports, and study delivery strategies. May act as departmental Subject Matter Expert (SME) for tools, processes and may act as Lead departmental development initiatives.
