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Associate Director, Clinical Science
eGenesis, Inc.Associate Director, Clinical Science at eGenesis responsible for planning and overseeing clinical development programs. Working collaboratively to ensure scientific integrity and operational excellence.
Posted 7/23/2026full-timeCambridge • Massachusetts • 🇺🇸 United StatesSenior💰 $175,000 - $226,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical development and translational science, with a strong focus on clinical trial design, regulatory submissions, and cross-functional collaboration. Proven ability to lead data analysis and ensure compliance with GCP guidelines and clinical R&D policies.
Highest-signal resume keywords
Clinical Development ExperienceClinical Trial DesignRegulatory SubmissionsData AnalysisCross-Functional Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ScienceClinical Protocol DevelopmentData Collection StandardsGCP GuidelinesAnalytical SkillsClinical Development PlansStudy ExecutionRegulatory ComplianceTranslational ScienceVendor Management
Soft Skills
Excellent CommunicationCollaboration SkillsLeadership Skills
Tools & Technologies
ExcelPowerPoint
Certifications & Qualifications
PharmDPhD
Industry Keywords
BiotechPharmaceuticalCROClinical R&DSOPsSafety ReportsEfficacy
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Support the design and implementation of early and late-stage clinical projects and ensure that the overall scientific and medical content of all clinical programs is scientifically and clinically rigorous
- Develop and maintain clinical development plans that integrate preclinical, translational, and clinical data while ensuring alignment across cross-functional teams
- Design scientifically rigorous, operationally feasible, and cost-effective clinical protocols aligned with the overall clinical development plan
- Present clinical protocols, development plans, and study updates to internal governance committees and senior leadership
- Serve as the Clinical Science representative on cross-functional project teams
- Partner closely with the Medical Monitor to oversee study conduct, monitor study progress, and ensure protocol compliance
- Lead data review, evaluation, and analyses in collaboration with Data Management and Biostatistics and Statistical Programming teams
- Contribute to the preparation of clinical sections of regulatory submissions and supporting documents, including INDs, briefing documents, BLAs, Safety and Annual reports, and responses to regulatory agencies regarding questions about clinical development issues (e.g., safety or efficacy)
- Ensure compliance with applicable regulations, clinical R&D policies, SOPs and quality standards
- Support scientific due diligence activities, including preparing and presenting medically-sound strategies and plans associated with advanced opportunities
- Drive continuous improvement to enhance Clinical Development processes, study execution and cross-functional collaboration
Requirements
What you’ll need- PharmD or PhD with 7+ years of clinical science experience in a biotech or pharmaceutical company, or CRO environment
- Experience in clinical development and/or translational science required
- Strong understanding of clinical trial design, data collection standards, and GCP guidelines
- Strong analytical skills with the ability to analyze and compile complex clinical data
- Strong experience working with vendors and clinical sites
- Excellent communication and collaboration skills with both internal teams and external partners
- Proven leadership skills and demonstrated ability to interact collaboratively in a cross-functional environment.
- Excellent oral and written communication skills, including proficiency with Excel and PowerPoint
Benefits
Comp & perks- 🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account eGenesis, Inc. Website LinkedIn All Job Openings 51 - 200 employees Founded 2015 🧬 Biotechnology ⚕️ Healthcare Insurance 💊 Pharmaceuticals Biotechnology
- Healthcare Insurance
- Pharmaceuticals eGenesis, Inc. is a biotechnology company focused on transforming the landscape of organ and therapeutic cell transplantation. By leveraging advanced genome engineering and multiplex gene editing technologies, eGenesis aims to develop human-compatible organs and cells, particularly through the innovative field of xenotransplantation. Their mission is to address the growing organ transplant shortage and improve the lives of patients in need, envisioning a future where no one has to suffer due to the lack of available organs. Associate Director, Clinical Science 🔥 1 hour ago 🏢🏡 Cambridge – Hybrid 💵 $175k - $226k / year ⏰ Full Time 🟠 Senior 👨⚕️ Medical Director Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
- Support the design and implementation of early and late-stage clinical projects and ensure that the overall scientific and medical content of all clinical programs is scientifically and clinically rigorous
- Develop and maintain clinical development plans that integrate preclinical, translational, and clinical data while ensuring alignment across cross-functional teams
- Design scientifically rigorous, operationally feasible, and cost-effective clinical protocols aligned with the overall clinical development plan
- Present clinical protocols, development plans, and study updates to internal governance committees and senior leadership
- Serve as the Clinical Science representative on cross-functional project teams
- Partner closely with the Medical Monitor to oversee study conduct, monitor study progress, and ensure protocol compliance
- Lead data review, evaluation, and analyses in collaboration with Data Management and Biostatistics and Statistical Programming teams
- Contribute to the preparation of clinical sections of regulatory submissions and supporting documents, including INDs, briefing documents, BLAs, Safety and Annual reports, and responses to regulatory agencies regarding questions about clinical development issues (e.g., safety or efficacy)
- Ensure compliance with applicable regulations, clinical R&D policies, SOPs and quality standards
- Support scientific due diligence activities, including preparing and presenting medically-sound strategies and plans associated with advanced opportunities
- Drive continuous improvement to enhance Clinical Development processes, study execution and cross-functional collaboration 🎯 Requirements
- PharmD or PhD with 7+ years of clinical science experience in a biotech or pharmaceutical company, or CRO environment
- Experience in clinical development and/or translational science required
- Strong understanding of clinical trial design, data collection standards, and GCP guidelines
- Strong analytical skills with the ability to analyze and compile complex clinical data
- Strong experience working with vendors and clinical sites
- Excellent communication and collaboration skills with both internal teams and external partners
- Proven leadership skills and demonstrated ability to interact collaboratively in a cross-functional environment.
- Excellent oral and written communication skills, including proficiency with Excel and PowerPoint 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 Senior Director, Medical Writing 🔥 1 hour ago Agomab 11 - 50 Website LinkedIn All Job Openings Senior Director overseeing regulatory documents for Agomab, a biotech company. Leading medical writing function and collaborating with cross-functional teams in a hybrid work environment. 🏢🏡 Cambridge – Hybrid ⏰ Full Time 🟠 Senior 👨⚕️ Medical Director Associate Director, Clinical Operations Compliance 🕒 July 7 Scholar Rock 51 - 200 Website LinkedIn All Job Openings Director of Clinical Operations Compliance at Scholar Rock focused on compliance for clinical programs. Leading oversight and adherence to standard procedures to ensure inspection readiness. 🏢🏡 Cambridge – Hybrid 💵 $175k - $225k / year 💰 $205M Post-IPO Equity on 2022-06 ⏰ Full Time 🟠 Senior 👨⚕️ Medical Director Senior Director, Clinical Operations 🕒 June 24 ARTBIO 51 - 200 Website LinkedIn All Job Openings Senior Director overseeing all aspects of clinical trial execution at ARTBIO, ensuring high-quality data and collaboration with cross-functional teams. 🏢🏡 Cambridge – Hybrid 💰 $90M Series A on 2023-12 ⏰ Full Time 🟠 Senior 👨⚕️ Medical Director Senior Medical Director, Clinical Safety 🕒 June 12 BlueRock Therapeutics 201 - 500 🧬 Biotechnology 💊 Pharmaceuticals 🔬 Science Website LinkedIn All Job Openings Clinical Safety Physician leading safety assessments for clinical trials at BlueRock Therapeutics. Collaborating with regulatory teams and overseeing safety operations for clinical drug development. 🏢🏡 Cambridge – Hybrid 💵 $310k - $365.8k / year 💰 $225M Series A on 2016-12 ⏰ Full Time 🟠 Senior 👨⚕️ Medical Director 🦅 H1B Visa Sponsor Senior Medical Director, Rare Hematology 🕒 May 20 Sanofi 10,000+ employees 💊 Pharmaceuticals 🧬 Biotechnology ⚕️ Healthcare Insurance Website LinkedIn All Job Openings Senior Medical Director overseeing the rare hematology portfolio for Sanofi in the U.S. Delivering strategic leadership and supporting patient care optimization through medical affairs. 🏢🏡 Cambridge – Hybrid 💵 $206.3k - $343.8k / year 💰 Post-IPO Equity on 2022-03 ⏰ Full Time 🟠 Senior 👨⚕️ Medical Director 🦅 H1B Visa Sponsor 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 Find jobs using your resume 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