Senior Medical Director

BBOT

Senior Medical Director overseeing clinical studies and leading cross-functional teams at Bridge Bio Oncology Therapeutics. Ensuring compliance with ethical and regulatory requirements while improving patient lives.

Posted 6/23/2026full-timeRemote • California • 🇺🇸 United StatesSenior💰 $266,500 - $319,000 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Serve as trial medical lead/medical monitor of assigned clinical studies, including contributing to site selection, study oversight and management plans, CRF design, ICF, enrollment, medical data review, CSR writing, and authoring of clinical modules and clinical review of other modules
Be a leader within and actively participate and contribute to the cross-functional and project teams meetings, including functioning as clinical representative
Cultivate relationships with clinical investigators, clinical consultants, and thought leaders for the execution of ongoing trials and developing opportunities
Help ensure Clinical Study Team compliance with ethical and GCP guidelines, and FDA, EMEA, ICH, and other regulatory requirements relevant to industry/country/region
Provide expert support for the preparation of clinical/study protocols and amendments, clinical trial documents
Responsible for the clinical sections of regulatory documents (investigator brochures, development safety update report, etc), clinical study reports
Conduct investigator meetings and lead site initiation visits with clinical trial investigators
Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
Translate findings from research and nonclinical studies into clinical development opportunities
Contribute to the clinical portions of writing and preparation of abstracts, presentations, and manuscripts
Attend key scientific congresses and meetings as requested in support of speakers and key opinion leaders
Remain current in relevant therapeutic areas and conversant with the literature as well as critical emerging data
Represent the Clinical Development team during interactions with regulatory agencies, as applicable

Requirements

What you’ll need

Trained MD and/or MD-Ph.D. degree
7+ years of experience in drug development, either within the industry or as a clinical investigator/physician-scientist in academia, or equivalent experience; oncology experience is preferred
Patient-focused, with a deep commitment to understanding needs and improving the lives of patients, and a passion for developing novel therapeutics
Demonstrated ability to collaborate successfully with multiple functions in a team environment
Demonstrated record of accomplishment in a compressed time frame; capable of prioritizing tasks and delivering on deadlines with high-performance standards and attention to detail
Motivated to work in a fast-paced, high accountability, small company environment; a "can do" and collegial professional who leads through influence and interpersonal skills
Intellectually curious with the courage to challenge and seek new ways to improve work
Strong written and oral communication skills, including presentation skills
Ability to analyze and interpret data and develop written reports and presentations of those data
Solid critical, strategic, and analytical thinking skills
Experience in all aspects of study and protocol conduct, both early and late phase, including protocol writing, start-up, study execution, analysis, and reporting
Experience in working closely with investigative sites, including principal investigators, sub-investigators, study coordinators, and other site personnel involved in clinical trials.

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account BBOT Website LinkedIn All Job Openings 51 - 200 employees 🧬 Biotechnology 💊 Pharmaceuticals Biotechnology
Pharmaceuticals BBOT is a biotechnology company developing targeted therapies for cancers driven by RAS signaling and PI3Kα. The company focuses on rational drug design to inhibit the active ON state of RAS and to selectively block RAS-driven PI3K activation, aiming at multiple KRAS mutants and novel approaches to maximize target inhibition. BBOT translates decades of RAS biology research into therapeutic candidates intended to improve outcomes for patients with RAS- and PI3Kα-driven tumors. Senior Medical Director Job not on LinkedIn 🔥 31 minutes ago 🏄 California – Remote 💵 $266.5k - $319k / year ⏰ Full Time 🟠 Senior 👨‍⚕️ Medical Director Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
Serve as trial medical lead/medical monitor of assigned clinical studies, including contributing to site selection, study oversight and management plans, CRF design, ICF, enrollment, medical data review, CSR writing, and authoring of clinical modules and clinical review of other modules
Be a leader within and actively participate and contribute to the cross-functional and project teams meetings, including functioning as clinical representative
Cultivate relationships with clinical investigators, clinical consultants, and thought leaders for the execution of ongoing trials and developing opportunities
Help ensure Clinical Study Team compliance with ethical and GCP guidelines, and FDA, EMEA, ICH, and other regulatory requirements relevant to industry/country/region
Provide expert support for the preparation of clinical/study protocols and amendments, clinical trial documents
Responsible for the clinical sections of regulatory documents (investigator brochures, development safety update report, etc), clinical study reports
Conduct investigator meetings and lead site initiation visits with clinical trial investigators
Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
Translate findings from research and nonclinical studies into clinical development opportunities
Contribute to the clinical portions of writing and preparation of abstracts, presentations, and manuscripts
Attend key scientific congresses and meetings as requested in support of speakers and key opinion leaders
Remain current in relevant therapeutic areas and conversant with the literature as well as critical emerging data
Represent the Clinical Development team during interactions with regulatory agencies, as applicable 🎯 Requirements
Trained MD and/or MD-Ph.D. degree
7+ years of experience in drug development, either within the industry or as a clinical investigator/physician-scientist in academia, or equivalent experience; oncology experience is preferred
Patient-focused, with a deep commitment to understanding needs and improving the lives of patients, and a passion for developing novel therapeutics
Demonstrated ability to collaborate successfully with multiple functions in a team environment
Demonstrated record of accomplishment in a compressed time frame; capable of prioritizing tasks and delivering on deadlines with high-performance standards and attention to detail
Motivated to work in a fast-paced, high accountability, small company environment; a "can do" and collegial professional who leads through influence and interpersonal skills
Intellectually curious with the courage to challenge and seek new ways to improve work
Strong written and oral communication skills, including presentation skills
Ability to analyze and interpret data and develop written reports and presentations of those data
Solid critical, strategic, and analytical thinking skills
Experience in all aspects of study and protocol conduct, both early and late phase, including protocol writing, start-up, study execution, analysis, and reporting
Experience in working closely with investigative sites, including principal investigators, sub-investigators, study coordinators, and other site personnel involved in clinical trials. Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score Similar Jobs Lead Senior Medical Director – DSNP 🕒 4 days ago CVS Health 10,000+ employees ⚕️ Healthcare Insurance 🛒 Retail 🧘 Wellness Website LinkedIn All Job Openings Lead Senior Medical Director at CVS Health, providing oversight for DSNP/FIDE populations. Drive medical management programs, ensuring compliance and improving outcomes across care continuum. 🇺🇸 United States – Remote 💵 $184.1k - $396.6k / year ⏰ Full Time 🟠 Senior 👨‍⚕️ Medical Director Pediatric Clinical Development Medical Director – Lead 🕒 5 days ago Pfizer 10,000+ employees Website LinkedIn All Job Openings Pediatric Clinical Development Medical Director Lead managing pediatric clinical programs across the U.S. Engaging with pediatric investigators and leading a specialized team to enhance site performance. 🇺🇸 United States – Remote 💵 $254.1k - $423.5k / year 💰 Post-IPO Debt on 2023-05 ⏰ Full Time 🟠 Senior 👨‍⚕️ Medical Director 🦅 H1B Visa Sponsor Medical Director – HIV Research, Clinical/Observational Research 🕒 6 days ago Syneos Health 10,000+ employees 🧬 Biotechnology 💊 Pharmaceuticals ⚕️ Healthcare Insurance Website LinkedIn All Job Openings Medical Director overseeing clinical studies and leading medical oversight at Syneos Health. Provides medical contact and input for project teams in clinical research settings. 🇺🇸 United States – Remote 💵 $146k - $277k / year ⏰ Full Time 🟠 Senior 👨‍⚕️ Medical Director 🦅 H1B Visa Sponsor Senior Medical Director – Medicaid 🕒 6 days ago CVS Health 10,000+ employees ⚕️ Healthcare Insurance 🛒 Retail 🧘 Wellness Website LinkedIn All Job Openings Senior Medical Director overseeing Medicaid for Aetna in the Northeast. Leading medical management activities and collaborating with health plan leaders across multiple states. 🇺🇸 United States – Remote 💵 $184.1k - $396.6k / year ⏰ Full Time 🟠 Senior 👨‍⚕️ Medical Director Senior Medical Director, Medical Affairs 🕒 June 16 Catalyst Pharmaceuticals, Inc. 51 - 200 🧬 Biotechnology 💊 Pharmaceuticals Website LinkedIn All Job Openings Senior Medical Director leading Medical Affairs strategy and execution for aGAMREE brand at Catalyst Pharmaceuticals. Collaborating cross-functionally to achieve objectives and timelines in a dynamic environment. 🇺🇸 United States – Remote 💵 $330k - $373k / year ⏰ Full Time 🟠 Senior 👨‍⚕️ Medical Director View More Medical Director Jobs 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

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Hard Skills & Tools

clinical study designCRF designICF designmedical data reviewCSR writingclinical protocol writingregulatory document preparationdata analysisclinical trial executionstudy oversight

Soft Skills

leadershipcollaborationcommunicationinterpersonal skillsattention to detailstrategic thinkinganalytical thinkingtime managementproblem-solvingintellectual curiosity

Certifications

MDMD-Ph.D.