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Clinical Scientist
vor 2 Monaten
Are you a talented Clinical Scientist with a passion for making a difference in the field of oncology and Phase 1 clinical trials? We have an exciting opportunity for you to join our renowned international life science partner based in Europe
Ashley Smith-Brown is working a well established CRO who are at the forefront of cutting-edge research and development in the life sciences industry. Our commitment to innovation, patient-centricity, and scientific excellence has enabled us to make significant strides in oncology and Phase 1 clinical studies. We work collaboratively with leading pharmaceutical companies, research institutions, and medical centres to bring ground breaking therapies to patients worldwide.
As a Clinical Scientist, you will play a pivotal role in designing, planning, and executing clinical studies in oncology and Phase 1 trials. You will work closely with cross-functional teams, including medical experts, statisticians, and data managers, to ensure the successful implementation of clinical protocols and deliver high-quality results. Your expertise and insights will contribute directly to advancing life-saving therapies and improving patient outcomes.
**Responsibilities**:
- Develop and review clinical trial protocols, informed consent forms, and study reports for oncology and Phase 1 studies.
- Collaborate with the medical team to provide scientific input during trial design and data analysis.
- Analyze and interpret clinical trial data, identify trends, and present findings to stakeholders.
- Ensure compliance with regulatory guidelines and industry best practices throughout the clinical trial process.
- Participate in investigator meetings, study site initiation visits, and monitoring activities.
- Contribute to the preparation of scientific publications and presentations for conferences.
**Qualifications**:
- Advanced degree (Ph.D., PharmD, or equivalent) in life sciences or related field.
- Proven experience in clinical research with a focus on oncology and Phase 1 trials.
- Strong understanding of GCP guidelines, clinical trial methodologies, and regulatory requirements.
- Excellent analytical and problem-solving skills.
- Collaborative team player with a results-oriented mindset.
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