At a Glance
- Tasks: Lead and manage clinical research projects, ensuring compliance and quality delivery.
- Company: Join Syneos Health, a top life sciences services organisation making a real impact.
- Benefits: Enjoy remote work, career development, and a supportive culture.
- Other info: Dynamic environment with opportunities for growth and mentorship.
- Why this job: Shape the future of healthcare while improving patients' lives globally.
- Qualifications: Degree in life sciences or related field; strong communication and project management skills.
The predicted salary is between 36900 - 45100 £ per year.
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 deliver – for one another, our customers, and, most importantly, for those in need.
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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
Job Responsibilities:
- Manages a project as Project Manager overseeing interdisciplinary clinical research programs ensuring compliance with Good Clinical Practices (GCPs), relevant Standard Operating Procedures (SOPs) and regulatory requirements.
- Acts as primary liaison between the Company and the Customer to ensure project launch, conduct, and closeout according to the Customer’s and the Company's contractual agreement.
- Leads clinical team to ensure quality, timelines and budget management.
- Accountable for the financial performance of assigned projects.
- Coordinates activities and deliverables of all project conduct partners and proactively identifies and manages issues.
Reporting and Communication:
- Accountable for maintenance of project information on a variety of databases and systems.
- Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools.
- Responsible for project management components of inspection readiness for all aspects of the project conduct, including Trial Master Files.
- Provides oversight for development and implementation of project plans in accordance with Controlled Documents.
- Independently prepares, coordinates, and presents project material at internal and external meetings.
- Directs the activities of assigned Project Support staff; line manages and mentors other project management team members and clinical staff; facilitates team building and communication.
- Prepares project management reports for clients and management.
- Implements resource strategies to achieve project goals.
- Develops contingency planning and risk mitigation strategies to ensure successful delivery of project goals.
Business Development:
- Participates in bid defense meetings where presented as potential project manager/director.
- Develops strong relationships with current clients to generate new and/or add-on business for the future.
- Keeps a current awareness of business unit’s and assigned projects’ therapeutic environment and drug development trends.
Qualifications:
- Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience.
- Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures.
- Clinical research organization (CRO) and relevant therapeutic experience preferred.
- Strong ability to manage time and work independently.
- Ability to embrace new technologies.
- Excellent communication, presentation, interpersonal skills, both written and spoken.
- Flexibility and the ability to mentor and manage new staff and to handle multiple tasks to meet deadlines delivering high quality work in a dynamic environment.
- Ability to travel as necessary (approximately 25%).
The position provides customer focused leadership in managing and delivering the operational and financial aspects of one or more clinical projects from proposal development to final deliverables and ranging in size and complexity from single service studies to full scope, multiple protocol projects and/or global projects across various phases and functional areas with limited interaction from supervisor. May oversee less experienced Project Managers (PMs) and have line management responsibilities.
A career with Syneos Health means your everyday work improves patients’ lives around the world.
Global Study Manager (Oncology )/ Sr PM - Sponsor-dedicated, EMEA countries in London employer: Syneos Health, Inc.
Syneos Health is an exceptional employer that prioritises employee growth and development, offering comprehensive benefits including health coverage, a 401k match, and flexible paid time off. Our inclusive work culture fosters collaboration among passionate professionals dedicated to making a meaningful impact in the healthcare sector, particularly in oncology clinical trials. By joining our remote team in Colorado, you will be part of a dynamic organisation that values innovation and empowers you to shape solutions that improve patients' lives globally.