Medical Director - Diabetes

SciPro; California (MO); Remote; USD 300,000 - 330,000; Full time

Job summary

An innovative firm is seeking a Medical Director to lead clinical development in metabolic assets. This role involves providing clinical expertise, guiding trial designs, and collaborating with cross-functional teams to enhance product safety and efficacy. The ideal candidate will have a strong background in diabetes and endocrinology, with a passion for advancing healthcare solutions. Join a dynamic team committed to pushing the boundaries of science and making a significant impact in the biotechnology field. If you are ready to take the next step in your career and contribute to groundbreaking research, this opportunity is for you.

Qualifications

• MD with board certification or eligibility required.
• 3+ years of experience in biotechnology or pharma industry.

Responsibilities

• Provide clinical/scientific knowledge for global evidence generation.
• Act as medical monitor during clinical trials execution.
• Oversee authoring of clinical study reports and regulatory submissions.

Skills

Clinical Development

Regulatory Interactions

Data Interpretation

Clinical Trials Design

Scientific Communication

Education

MD with board certification in Diabetes, Metabolism or Endocrinology

3+ years of clinical development experience

Job description

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Remote with Occasional Travel to Bay Area (Once a Month)

Consultant

Position Summary:

Responsibilities:

• Provide clinical/scientific knowledge into the development, design, delivery, and communication of the global evidence generation plan for multiple metabolic assets.
• Be able to plan, provide input and guidance to clinical trials design and implementation
• Support cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program
• Participate and provide clinical input into safety and regulatory interactions
• Act as medical monitor during clinical trials execution.
• Interpret and communicate clinical trial data
• Oversee the authoring of clinical study reports, publications, and regulatory submissions
• Develop relationships with key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by Global Development Lead
• Provide clinical content input to materials to be used in Scientific Affairs as well as the Commercial Organization
• Contribute to TPP (target product profile) and Global Product Safety (GPS) development
• Create development options and present to Global Dev Review Committee (GDRC), Therapeutic Area Governance (TAG)
• Interact with TA leadership and extended team to develop strategies options
• Interact with Center for Design Analysis (CfDA), Center for Observational Research (CfOR), Clinical Pharmacology Modeling & Simulation (CPMS), etc., to bring innovative later development options.

Education and Experience Requirements:

• MD with board certification or eligibility in Diabetes, Metabolism or Endocrinology
• 3+ years of clinical development experience in biotechnology or pharma industry
• experience in the design, execution, and reporting of controlled clinical trials in diabetes
• Experience with diabetes-related technology

Employment Type:

• Full-time contractor

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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