Director, Clinical Scientist – Respiratory Indications

🔥 12 hours ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $186k - $270k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Generate Biomedicines

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2020

🧬 Biotechnology

🤖 Artificial Intelligence

💊 Pharmaceuticals

💰 $370M Series B on 2021-11

Biotechnology • Artificial Intelligence • Pharmaceuticals

Generate Biomedicines is a pioneering therapeutics company that stands at the intersection of machine learning, biological engineering, and medicine. They are leading the development of generative biology, a groundbreaking approach that uses artificial intelligence to create novel medicines with specific therapeutic functions. By studying millions of proteins, Generate Biomedicines has discovered generalizable rules by which nature encodes function, enabling them to generate medicines on demand across multiple therapeutic modalities. Their innovative platform promises to fundamentally change the way medicines are made, expanding technical possibilities and improving speed and success rates in drug discovery.

📋 Description

• Serve as clinical science lead and core member of clinical development teams for respiratory studies • Support day-to-day study execution and alignment with protocols, timelines, and regulatory requirements • Design and develop clinical trial protocols and associated documents • Develop clinical components of regulatory documents • Review and interpret clinical data to ensure data quality, participant safety, and protocol compliance • Participate in site selection, initiation, and ongoing engagement • Track study progress, identify risks, and implement mitigation strategies • Serve as scientific contact for CROs and vendors • Collaborate with Clinical Operations, Regulatory, Biostatistics, Data Management, and Safety teams • Contribute to governance meetings, study updates, data summaries, and risk assessments • Maintain inspection readiness and support audits and inspections • Support publications, abstracts, and manuscripts • Contribute to TPPs, clinical development plans, and risk-benefit assessments • Support oversight committees for late-stage asthma studies • Mentor and coach team members where appropriate

🎯 Requirements

• Advanced degree (PhD, PharmD, MD, MS, PMP) • 9+ years of industry experience in clinical development • Direct experience in late-stage respiratory (asthma and/or COPD) studies • Strong knowledge of clinical research methodologies, regulatory guidelines, and GCP • Demonstrated ability to lead clinical science strategy and execution in late-stage trials • Excellent analytical, communication, and cross-functional collaboration skills • Prior experience authoring clinical protocols, CSRs, and regulatory documents

🏖️ Benefits

• Annual bonus • Equity compensation • Competitive benefits package • Remote work option in the U.S. with travel to HQ based on business needs