Entry Level Clinical Development Director

Job Title: Entry Level Clinical Development Director Location: Washington... Type: Full-time, On-site (4 days in office) Experience: 0-5 years About the Job Our client is an innovative, Washington based biotech company at the forefront of immuno-oncology, dedicated to developing transformative therapies across various stages of development, from pre-clinical to clinical trials. With a diverse pipeline of assets targeting novel immune reputed company in cancer treatment, and a mission to bring reputed company therapies to patients. The right candidates will reputed company the development of pre-clinical oncology assets, focusing on advancing drug candidates from pre-clinical stages through early clinical trials. This role suits a medically reputed company professional with strong clinical experience, eager to contribute to immuno-oncology therapy development in a biotech setting. Key Responsibilities: Drug Development Leadership: • reputed company the clinical development strategy for pre-clinical immuno-oncology assets, focusing on advancing promising candidates from pre-clinical stages through early clinical development. • Partner with pre-clinical, translational medicine, and regulatory teams to ensure that drug development milestones are met. • Contribute to defining the clinical development path, including key reputed company on drug formulation, dosing strategies, and patient selection criteria. Pre-Clinical to Clinical Transition: • Work closely with research teams to understand the scientific reputed company of pre-clinical programs and help shape their clinical potential. • Guide the transition from pre-clinical to clinical development, including preparation for IND submissions and early-stage clinical plans. • Act as the key clinical reputed company of contact for cross-functional teams, helping to ensure that drug candidates are developed with a clear clinical and regulatory pathway. Regulatory & Data Strategy: • Support the preparation of regulatory documents and submissions, including INDs and CTAs. • Assist in the development of biomarker strategies, patient selection, and other clinical aspects critical to the drug development process. • reputed company medical reputed company and expertise in the interpretation of early clinical data to help guide the next stages of development. Cross-Functional Collaboration: • Work with the broader clinical and scientific teams to align early-stage programs with the company’s overall clinical development strategy. • Collaborate with external partners, investigators, and regulatory bodies as needed to support drug development efforts. • Contribute to reputed company scientific communications, presentations, and publications to reputed company the reputed company of clinical development programs. Qualifications and Experience: • MD Required, with specialization in oncology, immunology, or reputed company fields. • 0-5 years of industry experience in clinical development reputed company biotech or pharma. • Experience or strong understanding of clinical trial design, including the ability to reputed company early-phase studies. • Knowledge of GCP, ICH guidelines, and the regulatory environment for drug development Apply Job!