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Lead Clinical Research Manager
2 months ago
Meet the challenges of a dynamic and innovative biopharmaceutical company as a seasoned clinical trial professional. We are dedicated to transforming lives through groundbreaking therapies.
Key Responsibilities:
- Oversee the planning, implementation, and management of clinical trials from start to finish, ensuring seamless execution and timely delivery.
- Develop and maintain study protocols, regulatory submissions, and compliance with Good Clinical Practice (GCP) guidelines, fostering a culture of excellence and quality.
- Collaborate with cross-functional teams, including clinical operations, data management, and regulatory affairs, to drive project success and achieve business objectives.
- Build and maintain relationships with external partners, such as Contract Research Organizations (CROs), investigators, and vendors, to ensure effective communication and coordination.
- Provide timely and accurate reporting of study results and progress to stakeholders, ensuring transparency and accountability.
- Identify and mitigate risks to ensure the successful execution of clinical trials, applying sound judgment and analytical skills.
- Mentor and guide junior team members, fostering a collaborative and high-performing work environment that promotes growth and development.
Qualifications:
- Bachelor's degree in a scientific discipline, such as biology, chemistry, or pharmacology.
- Minimum of 4 years of experience in clinical trial management, with a strong track record of leading Phase I-III trials and delivering results.
- Comprehensive understanding of clinical trial design, regulatory requirements, and GCP, with a focus on oncology or rare disease clinical trials.
- Excellent organizational, communication, and leadership skills, with the ability to work effectively in a fast-paced, dynamic environment.
- Strong problem-solving skills and attention to detail, with a commitment to quality and excellence.