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 and enhance your leadership skills in a global environment.
- 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.
Location: Home-based
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.
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based) in Reading employer: IQVIA Argentina
As an Associate Director Senior Study Lead at our company, you will thrive in a dynamic and supportive home-based environment that prioritises operational excellence and employee growth. We offer competitive compensation, comprehensive health benefits, and a culture that fosters collaboration and innovation, ensuring you have the resources and opportunities to excel in your career while making a meaningful impact in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based) in Reading
✨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 researching the company and its culture. Understand their recent projects and challenges in clinical trials. This will help you tailor your answers and show that you’re genuinely interested in being part of their team.
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience aligns with the Associate Director Senior Study Lead role. Highlight your leadership skills and your ability to manage complex studies effectively.
✨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 serious about 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) in Reading
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 Clinical Research Inside Out
Make sure you brush up on your knowledge of clinical research, especially Phases I to IV. Be ready to discuss your past experiences and how they relate to the role. Highlight any specific studies you've led and the outcomes achieved.
✨Showcase Your Leadership Skills
As an Associate Director Senior Study Lead, you'll need to demonstrate your ability to lead cross-functional teams. Prepare examples of how you've successfully managed virtual teams and resolved conflicts in a matrix environment. This will show your potential employer that you can handle the responsibilities of the role.
✨Be Agile and Proactive
Familiarise yourself with agile methodologies and be prepared to discuss how you've applied them in your previous roles. Emphasise your proactive approach to operational planning and risk management, as these are key aspects of the job.
✨Communicate Clearly and Effectively
Since excellent communication is crucial for this role, practice articulating your thoughts clearly. Prepare to present your ideas confidently, whether it's about study protocols or stakeholder relationships. Remember, being able to communicate at all levels is essential!
