Track This Job
Add this job to your tracking list to:
- Monitor application status and updates
- Change status (Applied, Interview, Offer, etc.)
- Add personal notes and comments
- Set reminders for follow-ups
- Track your entire application journey
Save This Job
Add this job to your saved collection to:
- Access easily from your saved jobs dashboard
- Review job details later without searching again
- Compare with other saved opportunities
- Keep a collection of interesting positions
- Receive notifications about saved jobs before they expire
AI-Powered Job Summary
Get a concise overview of key job requirements, responsibilities, and qualifications in seconds.
Pro Tip: Use this feature to quickly decide if a job matches your skills before reading the full description.
Accountabilities
- Leading local study teams to deliver clinical studies according to agreed resources, budget, and timelines.
- Ensuring proper site identification, qualification, setup, initiation, monitoring, closure, and documentation archiving.
- Conducting timely submissions of necessary applications/documents to Ethics Committees and Regulatory Authorities.
- Maintaining close communication with global study teams and managing study commitments.
- Creating and implementing alternative action plans to achieve targeted patient numbers and monitoring admission processes.
- Ensuring compliance with ICH-GCP practices and local regulations throughout the clinical research process.
- Participating in system/process improvement projects within global and local task groups.
- University degree in a healthcare-related field (Pharmacy, Veterinary, Chemistry, Biology, etc.).
- Advanced level of English.
- Minimum of 5 years of experience in Clinical Research, with at least 2 years in Project Management roles, preferably in Oncology.
- Strong project management skills.
- Excellent communication and negotiation skills.
- Ability to prioritize tasks and manage multiple responsibilities.
- Basic coaching skills and ability to work effectively in a team.
- Financial management skills.
- Effective planning and organizational skills with a results-oriented approach.
- Experience in stakeholder management.
- Strong analytical thinking and critical reasoning abilities.
- Proficient in MS Office applications.
- No travel restrictions.
- Valid driving license.
- Opportunity to work on impactful oncology studies.
- Remote work flexibility.
- Professional development and training opportunities.
- Collaborative work environment with global teams.
- Exposure to innovative clinical practices and strategies.
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Key Skills
Ranked by relevanceReady to apply?
Join Jobgether and take your career to the next level!
Application takes less than 5 minutes

