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Associate Medical Director/Medical Director

Join Iambic Therapeutics as an Associate Medical Director or Medical Director to oversee clinical trials and ensure patient safety.

Location
Remote - US
Compensation
Not disclosed
Level
director
Type
full time · Remote

Posted by employer 4 days ago

First seen on Joblaze 4 days ago

Last verified on the company career page 13 hours ago

What you'll build

  • Serve as the medical monitor for assigned clinical trials
  • Work closely with other functional areas within Research and Development
  • Ensure participant safety by reviewing adverse events
  • Provide guidance on patient eligibility and protocol adherence
  • Support interactions with regulatory agencies

Must have

  • MD or PharmD with clinical oncology experience
  • Experience as a medical monitor on a clinical trial
  • Excellent written and verbal communication skills

Nice to have

  • Experience in biotech/pharma oncology drug development
  • PhD with a minimum of 3 years of biotech or pharmaceutical experience
  • Creative problem-solving skills

AI in the day-to-day

Iambic is developing novel medicines using its AI-driven discovery and development platform.

Requirements

Experience
3+ years

Not disclosed in this posting: compensation, visa sponsorship.

Benefits

401k Match Gym Membership Unlimited PTO Health Insurance

Joblaze summary

The Associate Medical Director or Medical Director at Iambic Therapeutics will oversee the execution of phase 1 clinical trials while ensuring patient safety and regulatory compliance. This role requires expertise in clinical oncology and experience in biotech or pharmaceutical drug development, particularly as a medical monitor. Ideal candidates will have strong communication skills and the ability to collaborate effectively across various functional teams. Iambic, a clinical-stage company founded in 2020, emphasizes innovation through its AI-driven drug discovery platform.

Joblaze insights

Quick facts

Is the Associate Medical Director/Medical Director role remote?
Yes — Iambic Therapeutics lists this as a fully remote position.
How much experience is required?
At least 3 years of relevant experience for this Associate Medical Director/Medical Director role.
What seniority level is this role?
Iambic Therapeutics targets director candidates for this position.
Is this full-time or contract?
Full-time for this Associate Medical Director/Medical Director role at Iambic Therapeutics.

From the original posting

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.

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