Global Feasibility Specialist

**Description**

**Global Feasibility Specialist (clinical trials) Argentina/Brazil/Mexico/Peru Home Based**

Syneos Health® 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 easier to work with, but to make us easier to work for.

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 accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:
**WORK HERE MATTERS EVERYWHERE**

**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 our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we’re able to create a place where everyone feels like they belong.

**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 mínimal 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**

**What we’re looking for**
- 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
- 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

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