At a Glance
- Tasks: Lead Phase 1 clinical trials, ensuring smooth operations and compliance.
- Company: Join Syneos Health, a top biopharmaceutical solutions organisation making a real impact.
- Benefits: Flexible work in London, career development, and a supportive culture.
- Why this job: Be part of a team that changes lives through innovative research.
- Qualifications: 5+ years in clinical trial management; strong leadership and communication skills.
- Other info: Dynamic environment with opportunities for growth and collaboration.
The predicted salary is between 48000 - 72000 £ per year.
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.
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
- Oversee the development, coordination, and implementation of Phase 1 clinical research studies at the organization’s facilities, ensuring that all aspects of the trial are conducted efficiently and effectively.
- Collaborate with principal investigators, research subjects, client teams, investigators, and clinic operations teams to facilitate communication and coordination, ensuring that all parties are aligned and informed throughout the trial process.
- Plan logistics and resource usage for clinical trials, including the allocation of staff, equipment, and materials, to ensure that trials are conducted smoothly and without delays.
- Track study progress in alignment with project milestones, client deliverables, and budget, using project management tools and techniques to monitor and report on the status of the trial.
- Ensure compliance with applicable regulations globally and by region, including adherence to Good Clinical Practice (GCP) guidelines, ethical standards, and regulatory requirements, to maintain the integrity and quality of the trial.
- Manage a team of individual contributors and supervisors, providing strategic vision and tactical direction, setting goals and objectives, and monitoring performance to ensure that the team operates effectively and achieves its targets.
- Deliver operational results that have direct impact on immediate or short-term department outcomes, using data-driven decision-making and problem-solving skills to address challenges and optimize trial performance.
- Provide in-depth knowledge and skills within the scientific/technology or professional discipline, understanding the impact of work on related areas, and leveraging expertise to contribute to the advancement of the organization’s research objectives.
- Utilize practical knowledge in managing the execution of processes, projects, and tactics within the team, ensuring that all activities are conducted in accordance with established protocols and procedures.
Qualifications
- Bachelor’s degree in a relevant scientific or healthcare field; advanced degree preferred.
- Minimum of 5 years of experience in clinical trial management, with a focus on Phase 1 studies.
- Proven track record of managing clinical trials and delivering successful outcomes.
- Strong understanding of global and regional regulations related to clinical research.
- Excellent organizational, planning, and resource management skills.
- Ability to lead and manage a team, providing strategic vision and tactical direction.
Certifications
- Certified Clinical Research Professional (CCRP) or equivalent certification preferred.
- Project Management Professional (PMP) certification is a plus.
Necessary Skills
- In-depth knowledge of clinical trial processes and regulations.
- Strong leadership and team management skills.
- Excellent communication and collaboration abilities.
- Proficiency in project management and resource planning.
- Ability to analyze and interpret complex data.
- Strong problem-solving and decision-making skills.
Roles within the Clinical Trial Management job family at the M24 level are responsible for overseeing all aspects of Phase 1 clinical research studies at the organization’s facilities. This involves collaboration with the principal investigator, liaisons between research subjects, client teams, investigators, and clinic operations teams. The manager plans logistics and resource usage, tracks study progress in alignment with project milestones, client deliverables, and budget, and ensures compliance with applicable regulations globally and by region.
Roles within the Clinical Trial Management job family at the M24 level play a pivotal role in the successful execution of clinical trials, directly impacting the organization’s ability to deliver high-quality research outcomes. By managing a team of individual contributors and supervisors, the manager ensures that operational results have a direct impact on immediate or short-term department results. Their in-depth knowledge and skills within the scientific/technology or professional discipline contribute to the understanding of the impact of work on related areas. The manager’s strategic vision and tactical direction across the discipline and broader organization are crucial for achieving goals through the management of processes, policies, and performance of direct and indirect reports.
Core Focus
- Overseeing the development, coordination, and implementation of Phase 1 clinical research studies.
- Collaborating with principal investigators, research subjects, client teams, investigators, and clinic operations teams.
- Planning logistics and resource usage for clinical trials.
- Tracking study progress in alignment with project milestones, client deliverables, and budget.
- Ensuring compliance with applicable regulations globally and by region.
- Managing a team of individual contributors and supervisors.
- Delivering operational results that impact immediate or short-term department outcomes.
- Providing strategic vision and tactical direction across the discipline and broader organization.
Sr Clinical Trial Manager - (1-2 days a week in London, UK based only) employer: Syneos Health Careers
Contact Detail:
Syneos Health Careers Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr Clinical Trial Manager - (1-2 days a week in London, UK based only)
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trial space, attend industry events, and don’t be shy about asking for introductions. The more people you know, the better your chances of landing that dream job.
✨Tip Number 2
Prepare for interviews by researching Syneos Health and understanding their values and mission. Tailor your responses to show how your experience aligns with their goals. Remember, they want to see your passion for changing lives through clinical trials!
✨Tip Number 3
Show off your problem-solving skills during interviews. Be ready to discuss specific challenges you've faced in clinical trial management and how you overcame them. This will demonstrate your ability to think on your feet and deliver results.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in being part of the Syneos Health team.
We think you need these skills to ace Sr Clinical Trial Manager - (1-2 days a week in London, UK based only)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Sr Clinical Trial Manager. Highlight your experience in managing Phase 1 studies and any relevant certifications. We want to see how your background aligns with our mission at Syneos Health!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how you can contribute to our Total Self culture. Let us know what makes you a great fit for our team.
Showcase Your Leadership Skills: Since this role involves managing a team, be sure to highlight your leadership experience. Share examples of how you've successfully led teams in the past and how you plan to bring that expertise to Syneos Health.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Syneos Health Careers
✨Know Your Stuff
Make sure you brush up on your knowledge of Phase 1 clinical trials and the specific regulations that apply. Syneos Health values expertise, so be ready to discuss your previous experiences and how they relate to the role.
✨Show Your Leadership Skills
As a Sr Clinical Trial Manager, you'll need to demonstrate strong leadership abilities. Prepare examples of how you've successfully managed teams in the past, focusing on how you set goals, provided direction, and achieved results.
✨Communicate Clearly
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely, especially when discussing complex topics like project management tools or compliance with GCP guidelines.
✨Align with Their Culture
Syneos Health prides itself on its Total Self culture. Be prepared to discuss how you can contribute to a diverse and inclusive environment, and share personal experiences that reflect your ability to work collaboratively with different teams.