At a Glance
- Tasks: Lead drug development strategies and manage innovative projects in a dynamic environment.
- Company: Join IQVIA, a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy a competitive salary, remote work options, and opportunities for professional growth.
- Other info: Collaborate with top experts and engage in strategic business development activities.
- Why this job: Make a real impact on patient outcomes while working with cutting-edge pharmaceutical developments.
- Qualifications: 15-20 years of clinical research experience and strong leadership skills required.
The predicted salary is between 63000 - 77000 £ per year.
Location: Home-based in Europe
Job Overview:
- Manages a department or small unit.
- Provide leadership and advice on the development of optimum strategies for drug development, product lifecycle management and portfolio management to meet pharmaceutical and biotechnology customer goals.
- Provide medical, clinical, scientific, regulatory, and product development leadership and consultancy expertise to support strategic business activities and investment opportunities.
- Participate in all aspects of Strategic Drug Development and lead the implementation of mission, goals and objectives, development of policies, procedures and standards for the department.
- Provide thought leadership in pharmaceutical product development by preparing publications, white papers, and blogs in areas of expertise and by participating in scientific conferences and webinars, as appropriate.
Essential Functions:
- Evaluate and develop product development strategies for pharmaceutical products focusing on clinical-commercial convergence that encompasses all phases of development from discovery to market.
- Support engagements with regulatory authorities (e.g., FDA, EMA) on behalf of customers, across the lifecycle of drug development.
- Lead assessments of risk and probability of regulatory success and development of mitigations for candidate pharmaceutical products.
- Support the innovative development of compounds to maximize technical, regulatory, and commercial success.
- Strategic leadership of the development of regulatory submissions.
- Ensure high-quality, well-reasoned, objective deliverables that meet the highest standards of medical, ethical and scientific integrity and conduct.
- Assume the role of customer senior management as requested.
- Provide drug development expertise to support strategic business activities and investment opportunities.
- Assist in the development of programs to maximize the organization’s growth and profitability.
- Ensure Customer Satisfaction by working closely with Senior Management, CRO Operations, Therapeutic Units, and other Operations Heads.
- Serve as a key resource and participate in strategic business development activities.
- Provide internal and external therapeutic and pharmaceutical development-related educational services.
- Attend key scientific meetings/conferences and keep abreast of relevant scientific publications.
- Develop and maintain ongoing relationships with pharmaceutical and biotechnology companies, key opinion leaders.
- Compliance with all business office requirements for tracking time and effort.
Qualifications:
- Masters degree or higher or the equivalent combination of education, training and experience.
- Typically requires 15-20+ years relevant clinical research experience with multi-regional and global focus.
- Requires broad management and leadership knowledge to lead multiple job areas.
- Expertise in Excel and PowerPoint.
- Strong strategic thinking, analytical and communication skills.
- Client-focused and consultative approach for project management.
- Demonstrates a strong command of a variety of analytical and market research techniques.
- Grasps key issues quickly, understands the 'big picture', and links market research insights to larger business issues.
- Demonstrates excellent written and verbal communication skills.
- Has a strong commitment to quality.
- Has a proven track record of meeting or exceeding goals.
- Has broad management knowledge to lead teams.
- Has ability to influence others to accept practices and approaches.
Summary Location: Reading, Berkshire, United Kingdom; Lisbon, Portugal; Budapest, Hungary; Stockholm, Sweden; Athens, Greece; Barcelona, Spain; Prague, Czech Republic; Sofia, Bulgaria; Copenhagen, Denmark; Madrid, Spain; Bucuresti, Romania
Type: Full time
Senior Director, Drug Development in Reading employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Director, Drug Development in Reading
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like IQVIA. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like IQVIA.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like IQVIA. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what IQVIA is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Senior Director, Drug Development in Reading
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at IQVIA!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show IQVIA that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at IQVIA!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At IQVIA, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at IQVIA
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at IQVIA that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with IQVIA’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
