Auf einen Blick
- Aufgaben: Lead and manage global clinical trials, ensuring smooth operations and data management.
- Arbeitgeber: Join BeiGene, a rapidly growing company dedicated to fighting cancer through innovative research.
- Mitarbeitervorteile: Enjoy a collaborative work environment with opportunities for professional growth and development.
- Warum dieser Job: Make a real impact in the fight against cancer while working with passionate professionals.
- Gewünschte Qualifikationen: Master's or Doctorate degree with 10+ years in pharma and 5+ years managing clinical trials.
- Andere Informationen: We celebrate diversity and are committed to equal opportunity in the workplace.
Das voraussichtliche Gehalt liegt zwischen 72000 - 108000 € pro Jahr.
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
- Work with country or global teams to plan and implement Phase IV GMA-sponsored clinical trials, interventional or non-interventional.
- This includes all aspects of study management and oversight, including working with the CRO, engaging with non-GMA stakeholders for alignment, project management, data management, safety planning, etc.
Essential Functions of the Job:
- Create the global governance structure and implementation process for these studies.
- Build capabilities and infrastructure for GMA-sponsored studies; interventional and non-interventional.
- Build the templates, tracking and reporting process for these studies for leadership and non-GMA members.
- Create a global SharePoint site to house all required documents and oversee all data is added to the appropriate systems (GMA portal, ClinOps portal).
- Work with the responsible party (e.g., Country Medical Director, HEOR lead) to create the implementation and operations plan for a GMA-sponsored study.
- Create the governance structure and planning forum for each study.
- Manage and track study-specific activities and deliverables.
Education Required:
- Master’s or Doctoral level degree required.
Qualifications:
- Master’s or Doctorate level degree with 10+ years of experience in the pharmaceutical industry.
- 5+ years of experience in managing company-sponsored clinical trials within the pharmaceutical industry.
- Preferred: Experience conducting post-marketing company-sponsored trials (interventional & non-interventional).
- Experience managing a CRO, understanding of global regulatory requirements for company-sponsored trials.
- Detail-oriented, organized, excellent written & verbal communication skills.
- Able to function in a fast-paced environment, self-directed.
Computer Skills:
- Excel, PowerPoint, Project Management Software, Smartsheet, data management databases (e.g., CTMS), Veeva or similar.
We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
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Project Controls Manager Sisslerfeld (f / m / d), 100% Arbeitgeber: Bachem

Kontaktperson:
Bachem HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Project Controls Manager Sisslerfeld (f / m / d), 100%
✨Tip Number 1
Make sure to highlight your experience in managing clinical trials, especially post-marketing studies. This is crucial for the Project Controls Manager role, as it directly relates to the responsibilities outlined in the job description.
✨Tip Number 2
Familiarize yourself with the specific project management software mentioned in the job description, such as Smartsheet and CTMS. Being able to demonstrate proficiency in these tools during the interview can set you apart from other candidates.
✨Tip Number 3
Prepare examples of how you've successfully built governance structures and managed cross-functional teams in previous roles. This will showcase your ability to create the global governance structure required for GMA-sponsored studies.
✨Tip Number 4
Network with professionals in the pharmaceutical industry who have experience with GMA-sponsored trials. Engaging with them can provide insights and potentially valuable connections that could help you land the job.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Project Controls Manager Sisslerfeld (f / m / d), 100%
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Project Controls Manager position. Understand the essential functions and qualifications required, as this will help you tailor your application to highlight relevant experiences.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 10+ years of experience in the pharmaceutical industry and specifically your 5+ years managing company-sponsored clinical trials. Use specific examples that demonstrate your expertise in project management and collaboration with CROs.
Showcase Your Skills: Detail your proficiency in necessary computer skills such as Excel, PowerPoint, and project management software. Mention any experience with data management databases like CTMS or Veeva, as these are crucial for the role.
Craft a Strong Cover Letter: Write a compelling cover letter that reflects your passion for fighting cancer and your motivation to work at BeiGene. Make sure to connect your personal values with the company's mission and culture, showcasing how you can contribute to their goals.
Wie du dich auf ein Vorstellungsgespräch bei Bachem vorbereitest
✨Show Your Passion for Cancer Research
Make sure to express your genuine interest in fighting cancer during the interview. Share any relevant experiences or motivations that drive you to work in this field, as BeiGene values candidates who are passionate about their mission.
✨Demonstrate Your Project Management Skills
Be prepared to discuss your experience in managing clinical trials and how you've successfully implemented governance structures in previous roles. Highlight specific examples where you led projects, managed teams, or collaborated with stakeholders.
✨Highlight Your Technical Proficiency
Since the role requires familiarity with various software tools, be ready to talk about your experience with Excel, PowerPoint, and project management software. Mention any specific projects where you utilized these tools effectively.
✨Prepare for Behavioral Questions
Expect questions that assess your ability to function in a fast-paced environment and your organizational skills. Use the STAR method (Situation, Task, Action, Result) to structure your responses and provide clear examples of how you've handled challenges in the past.