At a Glance
- Tasks: Lead cross-functional clinical trial teams and manage studies from start to finish.
- Company: Dynamic pharmaceutical company focused on innovative drug development.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a collaborative team with global reach and excellent career advancement potential.
- Why this job: Make a real impact in clinical research while working from home.
- Qualifications: Bachelor's degree in life sciences and 4+ years in clinical research required.
The predicted salary is between 40000 - 90000 £ per year.
The Associate Director Senior Study Lead is the leader of the cross-functional clinical trial team (CTT). The role guides planning and management of assigned clinical study/studies from end-to-end to achieve objectives, including proactive operational planning, risk management, budget and people allocation, and promotion of operational excellence through process improvement and knowledge sharing.
Key Accountabilities
- Executes and delivers clinical studies; guides planning and decision making at study-level
- Acts as the CTT product owner with clear and focused duties and responsibilities per the agile ways of working
- Active member of a Clinical Operations community within the study leadership organization
- Promotes operational excellence in the shared development of global clinical study protocols, study reports, and other study‑related documents
Deliverables
- Patient recruitment, clinical data, study documentation and study reports
- Efficient delivery of the protocol, ICF, Monitoring Plan, and CSR in quality and on time
- Cost effective management of study budget
- Proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT
Key Expertise and Skillset
- Bachelor's degree in life sciences/healthcare (or clinically relevant degree) required; advanced degree strongly preferred.
- ≥ 4 years recent involvement in clinical research or drug development spanning Phases I to IV of standard to high complexity and priority.
- ≥ 3 years recent contribution to and accomplishment in all aspects of conducting clinical studies of standard to high complexity and priority in a global/matrix environment in a pharmaceutical industry or contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities.
- Experience managing people globally in a complex matrix environment preferred.
- Proven ability and strong experience leading virtual teams and building capabilities; effective stakeholder relationship development.
- Excellent communicator and presenter (oral and written); ability to communicate at all levels.
- Excellent organization and prioritization.
- Strong negotiation and conflict resolution skills and enterprise mindset, demonstrated by ability to drive aligned solutions.
- Fluent English, oral and written.
Please note this role is not eligible for the UK visa sponsorship. Please note: due sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.
The potential base pay range for this role, when annualized, is 217.800,00 zł - 521.000,00 zł. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based) employer: IQVIA Argentina
As an Associate Director Senior Study Lead at our home-based location in Reading, you will join a dynamic and innovative team dedicated to advancing clinical research. We pride ourselves on fostering a collaborative work culture that prioritises employee growth through continuous learning opportunities and mentorship, while also offering competitive compensation and comprehensive benefits. Our commitment to operational excellence and proactive risk management ensures that you will be part of impactful projects that contribute to the future of healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by practising common questions related to clinical trials and leadership. We recommend doing mock interviews with friends or using online platforms to get comfortable with articulating your experience and skills.
✨Tip Number 3
Showcase your expertise! When you get the chance to meet potential employers, be ready to discuss specific projects you've led or contributed to. Highlight your achievements in managing clinical studies and how you’ve driven operational excellence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team and contributing to our mission.
We think you need these skills to ace Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Associate Director Senior Study Lead role. Highlight your experience in clinical research and any leadership roles you've held. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can contribute to our team. Keep it engaging and relevant to the job description.
Showcase Your Achievements:When detailing your experience, focus on specific achievements that demonstrate your ability to lead clinical studies. We love numbers and results, so quantify your successes where possible!
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at IQVIA Argentina
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trials, especially Phases I to IV. Familiarise yourself with GCP/ICH guidelines and the roles of health authorities like the FDA and EMA. This will show that you're not just a candidate but someone who understands the industry inside out.
✨Showcase Your Leadership Skills
As an Associate Director Senior Study Lead, you'll be leading cross-functional teams. Prepare examples of how you've successfully managed virtual teams and resolved conflicts in the past. Highlight your ability to build relationships and drive aligned solutions, as this is crucial for the role.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills and operational planning abilities. Think of specific scenarios where you've had to manage risks or improve processes. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly.
✨Communicate Clearly and Confidently
Since excellent communication is key for this role, practice articulating your thoughts clearly. Whether it's discussing study protocols or presenting data, being able to convey complex information simply will set you apart. Don't forget to ask insightful questions about the company’s approach to clinical studies!