Remote Medical Director Clinical Development

We are an innovative biotechnology firm specializing in respiratory research, with a global team headquartered in the UK. Our dynamic company provides exciting opportunities for growth and development!

Join a thriving small biotech company and take advantage of unparalleled opportunities for professional growth.
Enjoy a comprehensive benefits package that rewards your hard work and dedication.
Thrill in the excitement of cutting-edge scientific discovery and innovation.
Receive a highly competitive compensation package that recognizes your talents and achievements.

We are seeking a highly motivated and experienced Medical Director Clinical Development to join our team in the Scientific industry. This is a permanent remote position that requires the candidate to have at least 5 years of relevant experience in clinical development, medical monitoring, and drug development. The ideal candidate should have a strong background in Respiratory, Safety, IND, NDA, fungal infections, lung, FDA, clinical research, MD, infectious disease, rare disease, Biotechnology, Pharmaceutical, protocol, late stage, pulmonary, critical care, .NET Core, phase 3, SAE, CRO, and GcP.

Responsibilities:

As a Medical Director Clinical Development, you will be responsible for leading the clinical development of our products. You will work closely with cross-functional teams to develop and execute clinical development plans, protocols, and regulatory strategies. Your responsibilities will include:

• Designing clinical studies and protocols that meet regulatory requirements and scientific objectives
• Overseeing clinical trials, including monitoring of safety and efficacy data and reviewing SAEs
• Collaborating with cross-functional teams, including clinical operations, regulatory affairs, medical affairs, and biostatistics
• Providing medical input into clinical development plans, study designs, and data analysis
• Interpreting clinical trial data and presenting findings to internal and external stakeholders
• Contributing to the preparation of regulatory documents, including INDs, NDAs, and BLAs
• Ensuring compliance with GcP, FDA regulations, and other relevant guidelines

Qualifications:

• MD degree with a specialty in Pulmonary, Critical Care, or Infectious Diseases
• At least 5 years of experience in clinical development and drug development
• Experience in Respiratory, Safety, IND, NDA, fungal infections, lung, FDA, clinical research, infectious disease, rare disease, Biotechnology, Pharmaceutical, protocol, late stage, pulmonary, critical care, .NET Core, phase 3, SAE, CRO, and GcP
• Strong knowledge of clinical trial design, execution, and interpretation of data
• Experience in medical monitoring and oversight of clinical trials
• Ability to work independently and collaboratively in a cross-functional team environment
• Excellent communication and interpersonal skills
• Strong attention to detail and ability to manage multiple projects simultaneously

If you are passionate about clinical development and want to make a difference in the lives of patients, we encourage you to apply for this exciting opportunity.