Senior Clinical Project Manager. Home based in Spain. Sponsor dedicated.
Updated: Yesterday
Location: ESP-Remote (Madrid)
Job ID: 25102490
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.
Discover what our 29,000 employees, across 110 countries already know:
* We are passionate about developing our people through career development and progression; supportive 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
Project Manager responsible for the overall execution of clinical trial(s); from study concept through study completion.
May have direct reports and will matrix manage assigned study team(s) to ensure compliance and execution on timelines and deliverables.
Is aware of both internal and external business environments, assess impact on clinical studies and make modifications as necessary.
Escalates performance issues to management with plans for resolution.
Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
Manages the implementation, on-time execution and conduct of clinical study(ies); including the development of the Study Plan which includes key milestones, timelines; study costs, vendor selection and resource needs as well as ensuring quality and compliance.
Provides input on regulatory documents (e.g., Investigator’s Brochure (IB), CSR, and the IND/DSUR).
Effectively communicates study progress and actively identifies issues that potentially impact evaluable study data, ethical study conduct and ICH compliance and identify potential interventions or solutions to manage the issues.
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.
Summary
Project Manager overseeing the end-to-end execution of clinical trials, ensuring compliance, quality, timelines, and budget adherence while leading study teams, managing vendors, and proactively addressing operational and regulatory challenges.
Contact
Phone: 919 876 9300
Fax: 919 876 9360
Toll-Free: 866 462 7373
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 reasonable accommodation to complete any part of our application process, including the use of this website, please contact us at: Email: jobs@syneoshealth.com
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