Attovia Therapeutics
Medical Director
San Carlos, CA · Director
Sponsorship not specified$280k-$315kDetected 86 days ago
StatisticsProject ManagementClinical TrialsPharmacologyLeadershipCommunicationCollaborationPublic SpeakingAdaptability
About the role
- Attovia's rapidly expanding pipeline includes multiple first-in-human and early proof-of-concept studies for immune-mediated diseases.
- Conduct regular medical safety data reviews.
- Qualifications - MD with a minimum of 4 years of clinical drug development.
Responsibilities
- Lead cross-functional study teams in the design, implementation, analysis, and interpretation of clinical trials. Ensure that project deliverables are accomplished on time and within budget.
- Prepare and deliver presentations and other scientific communications for internal and external stakeholders, including clinical advisors and study investigators.
- Partner with Clinical Science and Clinical Operations to identify and build strong professional relationships with study investigators.
- Partner with Clinical Operations to identify, select, and manage CROs, study sites, and clinical vendors.
- Partner with Project Management to ensure that clinical activities, timelines, and budgets are aligned with overall corporate goals.
- Lead cross-functional study teams in the design, implementation, analysis, and interpretation of clinical trials.
- Identify, manage, and communicate potential safety signals.
- Proven track record of successful design and implementation of clinical trials.
Requirements
- MD with a minimum of 4 years of clinical drug development.
- Ability to work in a fast-paced, small biotech environment.
- Demonstrated leadership presence, with the ability to foster relationships with key opinion leaders, study investigators, and academic collaborators.
- Strong analytical skills with the ability to interpret complex data sets and make informed decisions.
- Familiarity with the general principles of pharmacology/toxicology as it relates to first-in-human studies and early drug development.
- MD with a minimum of 4 years of clinical drug development. Active medical license preferred.
- Ability to interpret medical safety data independently without additional oversight.
- Exceptional written and verbal communication skills as evidenced by publications and platform presentations at scientific meetings.
- Proven track record of successful design and implementation of clinical trials. Prior experience in early-stage drug development (Phase 1 to 2) strongly preferred.
- Therapeutic experience in immune-mediated diseases. Expertise in inflammatory bowel disease is preferred but not required.
- Proactive personality, positive/solution-oriented mindset, careful attention to detail, adaptability to rapidly changing environment, and high ethical standards.
- Willingness to travel intermittently for conferences, investigator meetings, and advisory boards.
- Willingness to work in-office at least 4 days per week and relocate if necessary.
- About Attovia
- Attovia is creating a pipeline of biotherapeutics with initial focus immune-mediated disease. The company leverages Attobody™, a novel biologics platform, to generate small format biparatopic binders that expand the addressable target universe across disease areas and can offer stronger efficacy, faster speed to response, and an improved safety profile than traditional approaches. We are currently progressing multiple programs across immune-mediated disease indications.
Nice to have
- Prior experience in early-stage drug development (Phase 1 to 2) strongly preferred.
- Therapeutic experience in immune-mediated diseases.
- Expertise in inflammatory bowel disease is preferred but not required.
Compensation
- $280k-$315k
Benefits
- Act as the medical monitor for Attovia clinical trials.
- Engage with key opinion leaders to gain medical insights, inform clinical development plans, and build awareness and enthusiasm for Attovia's programs.
- Serve as the medical knowledge expert in target indication(s), develop target product profiles, and contribute to clinical and regulatory strategy.
- Active medical license preferred.
Company info
- Integrity
- Learning & Growth
- Drive for Excellence
- Innovation
- Teamwork & Collaboration
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