Are you a seasoned clinical trial professional looking for a new challenge? Join this dynamic and innovative biopharmaceutical company, where they are dedicated to transforming lives through groundbreaking therapies.
Key Responsibilities:
- Lead the planning, implementation, and management of clinical trials from start to finish.
- Oversee study protocols, regulatory submissions, and compliance with Good Clinical Practice (GCP) guidelines.
- Coordinate with cross-functional teams, including clinical operations, data management, and regulatory affairs.
- Manage relationships with external partners, such as CROs, investigators, and vendors.
- Ensure timely and accurate reporting of study results and progress to stakeholders.
- Identify and mitigate risks to ensure the successful execution of clinical trials.
- Mentor and guide junior team members, fostering a collaborative and high-performing work environment.
Qualifications:
- Bachelor’s degree in a scientific discipline.
- Minimum of 4 years of experience in clinical trial management, with a strong track record of leading Phase I-III trials.
- Comprehensive understanding of clinical trial design, regulatory requirements, and GCP.
- Excellent organizational, communication, and leadership skills.
- Ability to work effectively in a fast-paced, dynamic environment.
- Strong problem-solving skills and attention to detail.
- Experience with oncology or rare disease clinical trials is a plus.
