At a Glance
- Tasks: Lead the start-up of clinical trials and drive innovative biotech therapies forward.
- Company: Join a pioneering biotech firm dedicated to transforming healthcare.
- Benefits: Competitive salary, professional development, and the chance to make a real impact.
- Other info: Collaborative environment with opportunities for process improvement and career growth.
- Why this job: Shape the future of biotech research and help deliver life-changing therapies.
- Qualifications: 5+ years in clinical research with strong project management skills.
The predicted salary is between 60000 - 80000 £ per year.
Are you a seasoned clinical professional passionate about advancing cutting‑edge biotech therapies? Join our innovative biotech client as a Study Start Up Oversight Lead, where you’ll be at the forefront of accelerating clinical trial initiation and bringing transformative medicines to patients faster. This pivotal role offers the opportunity to shape the future of biotech research through strategic oversight, process harmonization, and expert leadership across multiple studies.
Required Skills
- B.A. or B.S. in a scientific discipline; advanced degree preferred
- Minimum of 5 years of clinical research experience, with at least 3 years managing Study Start Up activities within a sponsor or biotech environment
- Proven track record in managing outsourced clinical trials, ensuring quality, timelines, and budgets are met
- Strong project management capabilities with proficiency in MS Project
- Advanced Excel skills
- Experience with Veeva CTMS and Study Start Up modules is highly desirable
- Comprehensive knowledge of international guidelines such as ICH‑GCP; basic understanding of GMP and GDP
- Exceptional organizational, communication, and interpersonal skills
- Effective negotiator capable of thriving in a matrixed, collaborative setting
Nice To Have Skills
- Experience working with CROs or investigator sites, including site management or monitoring
- Involvement in feasibility assessments, site contracting, budgeting, vendor setup, or informed consent processes
- Background in developing process templates, project materials, or implementing process improvements
Preferred Education And Experience
- Bachelor’s degree in a scientific discipline; advanced degrees or certifications such as CRA, PMP, or equivalent preferred
- Extensive clinical research background emphasizing Study Start Up oversight in biotech or sponsor environments
Other Requirements
- Proficiency in MS Project and advanced Excel
- Ability to lead cross‑functional teams and foster collaborative relationships
- Willingness to support and develop process improvements and special projects
- Availability for strategic calls, including scheduled and ad‑hoc meetings
Join our biotech client’s mission to revolutionize healthcare—bring your expertise in trial start‑up excellence and help deliver life‑changing therapies worldwide. If you’re ready to make an impact, apply now and become a key driver in innovative clinical research!
Study Start Up Oversight Lead in Maidenhead employer: Planet Pharma
Join our innovative biotech client as a Study Start Up Oversight Lead, where you will be part of a dynamic team dedicated to advancing cutting-edge therapies. The company fosters a collaborative work culture that prioritises employee growth and development, offering opportunities for professional advancement in a fast-paced environment. With a commitment to revolutionising healthcare, this role not only allows you to make a meaningful impact but also provides unique advantages such as access to the latest technologies and a supportive network of experts in the field.
StudySmarter Expert Advice🤫
We think this is how you could land Study Start Up Oversight Lead in Maidenhead
✨Network Like a Pro
Get out there and connect with folks in the biotech scene! Attend industry events, webinars, or even local meetups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Show Off Your Skills
When you land that interview, be ready to showcase your project management skills and experience with Study Start Up activities. Use specific examples from your past roles to demonstrate how you've successfully managed timelines and budgets.
✨Ask Smart Questions
During interviews, don’t just wait for them to ask you questions. Prepare some insightful ones about their processes or challenges they face in clinical trials. This shows you're genuinely interested and have done your homework!
✨Apply Through Our Website
Make sure to apply directly through our website for the best chance at landing that role. We love seeing candidates who take the initiative and are excited about joining our mission to revolutionise healthcare!
We think you need these skills to ace Study Start Up Oversight Lead in Maidenhead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Study Start Up Oversight Lead role. Highlight your clinical research experience, especially in managing Study Start Up activities, to show us you’re the right fit.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you’re passionate about biotech and how your background aligns with our mission. Be specific about your achievements in project management and oversight.
Showcase Your Skills:Don’t forget to mention your proficiency in MS Project and Excel, as well as any experience with Veeva CTMS. We want to see how your technical skills can contribute to our innovative projects!
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 don’t miss out on any important updates during the process!
How to prepare for a job interview at Planet Pharma
✨Know Your Stuff
Make sure you brush up on your clinical research knowledge, especially around Study Start Up activities. Familiarise yourself with international guidelines like ICH-GCP and be ready to discuss how you've applied these in your previous roles.
✨Showcase Your Project Management Skills
Be prepared to talk about your experience with project management tools like MS Project and Excel. Have specific examples ready that demonstrate how you've managed timelines, budgets, and quality in past clinical trials.
✨Highlight Your Leadership Experience
This role requires strong leadership in a collaborative setting. Share instances where you've led cross-functional teams or improved processes. Emphasise your ability to negotiate and foster relationships with CROs or investigator sites.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to biotech innovation and their expectations for the Study Start Up Oversight Lead. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
