Associate Medical Director/Medical Director
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What you'll do
- Serve as the medical monitor for assigned clinical trials, providing medical and scientific expertise throughout the study lifecycle.
- Work closely with other functional areas within Research and Development (clinical operations, regulatory sciences, data management, biostatistics, clinical pharmacology, nonclinical) to facilitate the execution of clinical trials and ensure that high standards of study conduct are met
- Ensure participant safety by reviewing adverse events (AEs), serious adverse events (SAEs) and protocol deviations collaborate with pharmacovigilance to assess safety signals across the study
- Provide guidance on patient eligibility and protocol adherence
- Contribute to preparation of study-related documents including study protocols and amendments, Investigator Brochures (IBs), informed consent forms (ICFs), and clinical study reports (CSRs)
- Review and interpret clinical trial data, ensuring accuracy and consistency in the safety, efficacy and other data
- Support interactions with regulatory agencies, including preparation of documents for submission and participation at regulatory meetings
- Establish strategic partnerships with KOLs, centers of excellence, and patient advocacy organizations
- Develop content for advisory board meetings
- Prepare abstracts and presentations for scientific symposia and manuscripts for publication in high impact peer reviewed journals
- Keep up to date on standard of care and experimental therapies in relevant clinical areas through familiarity with literature, attendance at meetings, conventions and professional associations
What they're looking for
- MD or PharmD with clinical oncology experience as well as experience in biotech/pharma oncology drug development is preferred.
- PhD with a minimum of 3 years of biotech or pharmaceutical experience in oncology drug development.
- Experience as a medical monitor on a clinical trial, including patient eligibility review, site interaction to oversee protocol adherence, protocol deviation review, clinical data review and cleaning activities, coding
- Experience in executing on clinical studies, including interactions with regulatory agencies
- Excellent written and verbal communication skills
- Ability to work effectively in cross functional teams with internal and external partners
- Excellent organizational and time management skills with strong attention to detail, and proven ability to handle multiple tasks efficiently and effectively.
- Creative problem-solving skills with proven ability to act in a proactive manner
Nice to have
- MD or PharmD with clinical oncology experience as well as experience in biotech/pharma oncology drug development is preferred.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
JOB SUMMARY
Iambic Therapeutics is seeking an Associate Medical Director or Medical Director to join its growing Clinical Development team. This position will be responsible for study execution and oversight of a clinical program currently in phase 1, as well as supporting pipeline programs that are in the preparation phase for IND submission. In addition to providing medical oversight for the phase 1 clinical trial, ensuring patient safety, regulatory compliance and scientific integrity, this individual will also contribute to the clinical program strategy and execution.
KEY RESPONSIBILITIES
Serve as the medical monitor for assigned clinical trials, providing medical and scientific expertise throughout the study lifecycle.
Work closely with other functional areas within Research and Development (clinical operations, regulatory sciences, data management, biostatistics, clinical pharmacology, nonclinical) to facilitate the execution of clinical trials and ensure that high standards of study conduct are met
Ensure participant safety by reviewing adverse events (AEs), serious adverse events (SAEs) and protocol deviations collaborate with pharmacovigilance to assess safety signals across the study
Provide guidance on patient eligibility and protocol adherence
Contribute to preparation of study-related documents including study protocols and amendments, Investigator Brochures (IBs), informed consent forms (ICFs), and clinical study reports (CSRs)
Review and interpret clinical trial data, ensuring accuracy and consistency in the safety, efficacy and other data
Support interactions with regulatory agencies, including preparation of documents for submission and participation at regulatory meetings
Establish strategic partnerships with KOLs, centers of excellence, and patient advocacy organizations
Develop content for advisory board meetings
Prepare abstracts and presentations for scientific symposia and manuscripts for publication in high impact peer reviewed journals
Keep up to date on standard of care and experimental therapies in relevant clinical areas through familiarity with literature, attendance at meetings, conventions and professional associations
QUALIFICATIONS
MD or PharmD with clinical oncology experience as well as experience in biotech/pharma oncology drug development is preferred. PhD with a minimum of 3 years of biotech or pharmaceutical experience in oncology drug development.
Experience as a medical monitor on a clinical trial, including patient eligibility review, site interaction to oversee protocol adherence, protocol deviation review, clinical data review and cleaning activities, coding
Experience in executing on clinical studies, including interactions with regulatory agencies
Excellent written and verbal communication skills
Ability to work effectively in cross functional teams with internal and external partners
Excellent organizational and time management skills with strong attention to detail, and proven ability to handle multiple tasks efficiently and effectively.
Creative problem-solving skills with proven ability to act in a proactive manner
ABOUT IAMBIC THERAPEUTICS
Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at iambic.ai.
MISSION & CORE VALUES
Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies.
PAY AND BENEFITS
We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team. We are in a brand-new state-of-the art facility in beautiful San Diego with an onsite gym, dining, and easy access to great places to live and play.
Company
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