Description
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.
Responsibilities
Job responsibilities
The RSL will establish, cultivate, and maintain scientific relationships with investigators and study coordinators to support enrollment while developing a strong understanding of clinical practice as it relates to areas of interest. This position interacts with various internal and external stakeholders, with focus on institutions and their alliance partners (if applicable), study coordinators, cell lab technicians and managers, clinical research associates, and investigators. This role will initially focus on clinical trials and study site engagement.
- Establishes and maintains strong working relationships with Principal Investigators (PIs), Study Coordinators and clinical trial sites to support the enrollment and conduct of our client’s clinical studies
- Identify appropriate patients and their treating physicians, support acceleration of clinical studies completion through identification of new clinical sites, collaboration with existing sites, and/or enrollment of appropriate patients in client-sponsored clinical trials.
- Works with our client Clinical Development and Clinical Operations leads and trial sites to understand and implement study protocols effectively with the aim to accelerate recruitment and enrollment activity
- Partners with sites to develop and implement effective local and regional subject recruitment strategies, suggest local outreach options, facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies
- Delivers medical / scientific education, based on study specific engagement plan, as required, to trial sites and provides input to key internal stakeholders on training materials for clinical trials, therapeutic areas, and disease state as outlined by our client; suggest and support implementation of local outreach options
Requirements
Along with a results-oriented mindset, self-assurance, and an engaging manner, the ideal candidate has:
- Advanced science degree required (PhD, PharmD, MD, NP, PA or equivalent), MD, PhD, PharmD highly preferred relevant clinical trial experience
- Experience in an inflammatory disease state(s) required, with SLE experience preferred
- Proven ability to interact with Key Opinion Leaders and all HCPs
- Experience in clinical research, patient recruitment, or investigational site management
- Must be able and have flexibility to travel
- Knowledge of clinical trial/research design, conduct and understanding clinical study results
Qualifications
What we’re looking for
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.
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.
