At a Glance
- Tasks: Lead clinical operations and drive impactful projects in the biopharma industry.
- Company: Join a global CRO dedicated to innovative solutions and improving lives.
- Benefits: Inclusive culture, career growth, and the chance to make a real difference.
- Other info: Dynamic environment fostering creativity and collaboration.
- Why this job: Be part of a team that transforms clinical trials and enhances patient outcomes.
- Qualifications: 8+ years in clinical research with management experience; CNS trial knowledge required.
The predicted salary is between 59400 - 72600 £ per year.
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
What Clinical Operations Site Management does at Worldwide:
- Embark on a fulfilling Clinical Operations career as you leave a lasting impact on patients’ lives.
- Provide therapeutic and operational expertise throughout the program/project delivery lifecycle.
- Ensure that projects within the Franchise are properly resourced.
- Collaborate with the Therapeutic team to provide effective delivery strategies and solutions for Franchise projects and programs.
- Act as main contact person for the Project management Franchise Lead.
- Present at Proposal Defense/client meetings as needed to support new or ongoing business.
- Ensure LCRAs are trained to support the clinical scope of work (which includes SOP review, QI/CAPA understanding, Clinical Monitoring Plan).
- Coordinate and collaborate with Worldwide Global Quality Assurance to provide training opportunities identified in CAPA information.
- Coordinate efforts between the Project Management, Site Management, and Study Start Up.
- Establish regular communication to include quality metrics and overall “health” of the projects.
- Conduct appraisal performance review for direct reports.
What you will bring to the role:
- Broad protocol knowledge; therapeutic knowledge desired.
- Comprehensive global knowledge, awareness, and practical understanding of the biopharma industry, drug development lifecycle and operational clinical trial delivery.
- Innovative and strategic thinker.
- Superior oral and written communication skills.
- Strong planning and organizational skills.
- Experienced problem solving/decision making skills.
Your background:
- 4-year college curriculum with a major concentration in biological, physical, health, pharmacy or other related science and 8 years clinical research experience as a clinical research associate OR equivalent education/training and 10 years clinical research experience as a clinical research associate.
- At least 2 years of management experience.
- Experience with CNS trials is required for this role.
We love knowing that someone is going to have a better life because of the work we do.
Senior Manager, Clinical Operations Site Management (Franchise Lead) - CNS - Europe employer: Worldwide Clinical Trials
Worldwide Clinical Trials is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals passionate about clinical research. With a strong emphasis on employee growth, the company offers numerous opportunities for skill development and career advancement, all while working in a diverse environment that values creativity and teamwork. Located in a vibrant area, employees benefit from a supportive atmosphere that encourages meaningful contributions to patient engagement activities.
