Updated: Yesterday
Location: ESP-Remote (Madrid)
Job ID: 25102409
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:
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
Lead studies in late phase, phase 2–3 protocols and support main studies in phase 3:
International trial registry (IRT)
Electronic case report form (eCRF) management
Data monitoring committee (DMC) set‐up
Study risk management plan (SRMP)
Prepare statistical analysis plans (SAPs), tables, listings and figures
Review specifications and perform statistical surveillance (STS), reviewing blinded data and conducting 2–3 STS meetings during study life
Recruiting the right patients?
Data look okay?
Assess statistical assumptions
Handle intercurrent events, SAS or R programming, and partial programming of efficacy.
Provide support across all assigned statistical tasks during the lifecycle of the project, from protocol to clinical study report (CSR).
Coordinate the activities of biostatistics and statistical programming personnel, ensuring timely completion of high‐quality work.
Prepare statistical analysis plans (SAPs) and collaborate with sponsor as required.
Serve as a biostatistics representative on project teams, interfacing with other departmental project team representatives.
Lead projects involving integrated analyses, attend regulatory agency meetings and respond to questions as needed.
Analyze data quality, conduct signal detection, trend analyses and support the reporting of clinical study results.
Maintain well‐organized, complete, and up‐to‐date project documentation, ensuring inspection readiness.
Support business development activities such as proposals, budgets and sponsor bid defense meetings.
Coach and mentor other biostatistics staff.
Perform other work‐related duties as assigned; minimal travel may be required.
Equal Opportunity Employer
Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires a reasonable accommodation to complete any part of our application process, please contact us at jobs@syneoshealth.com
Phone: 919 876 9300
Fax: 919 876 9360
Toll-Free: 866 462 7373
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