Global Feasibility Consultant
hace 3 días
**About Syneos Health**
We are a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Our mission is to translate unique clinical, medical affairs, and commercial insights into outcomes that address modern market realities.
Our Clinical Development model puts the customer and the patient at the center of everything we do. We strive to simplify and streamline our work to make Syneos Health easier to work with and to work for.
Whether you join us as a Functional Service Provider or in a Full-Service environment, you'll collaborate with passionate problem solvers who innovate as a team to help our customers achieve their goals. We're agile and driven to accelerate the delivery of therapies because we're passionate about changing lives.
Discover what our 29,000 employees across 110 countries already know: WORK HERE MATTERS EVERYWHERE.
**Why Choose Us**
We're dedicated to developing our people through career development and progression, supportive and engaged line management, technical and therapeutic area training, peer recognition, and total rewards programs. We're committed to our Total Self culture – where you can be authentically yourself. Our Total Self culture unites us globally, and we're dedicated to taking care of our people.
**Job Responsibilities**
- You'll work under guidance and supervision to assess data requirements and approaches for RFPs and individual paid feasibility assessments.
- Manage a limited number of project assignments of minimal to moderate complexity under the supervision of a line manager or delegate.
- Respond to standard, routine requests in consultation with a line manager or designee and apply data, knowledge/skills to outlined, known data collection activities.
- Liaise with internal stakeholders to review sponsor requirements, protocol, and timelines for individual RFPs under guidance and supervision of a line manager or delegate.
- Conduct guided research of scientific literature using the 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 robust feasibility preparation.
- Maintain comprehensive records of work and store all relevant data within internal libraries in a timely manner as per outlined processes.
- Develop relationships with internal and external stakeholders to establish clear communication methods.
**Requirements**
**What We're Looking For**
- A Bachelor's degree in Science with an emphasis in medical research
- Nominal experience in science or a related field
- Attention to detail in analysis and presentation of data
- Flexibility, creativity, and openness to suggestions
- Self-motivation and ability to work independently and as part of a critical team
- 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 and 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, and work collaboratively as part of a team
- Travel may be required, typically less than 5%
**Compensation and Benefits**
We offer a competitive salary of $65,000 - $85,000 per year, depending on experience, and a range of benefits to support your career growth and well-being, including opportunities for professional development, health insurance, retirement plans, and more.
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