Clinical Development Director

Enveda

. Own studies end to end as clinical lead, from protocol through start-up and enrollment .

Posted 11/10/2026full-timeRemote • United StatesLead💰 $225,000 - $250,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical study leadership, including protocol writing, regulatory documentation, and data-driven decision-making. Strong ability to collaborate with cross-functional teams and maintain a patient-first approach in clinical development.

Highest-signal resume keywords

Clinical Study LeadershipProtocol WritingData-Driven Decision MakingAI Utilization in Clinical WorkCollaboration with Investigators and KOLs

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Development ExperienceProtocol Writing as Primary AuthorStudy Management from Protocol to Database LockEndoscopic Endpoints KnowledgeData Analysis and Interpretation

Soft Skills

Collaborative ApproachDirect CommunicationHigh AgencyPatient-First Mindset

Tools & Technologies

AI Tools for Clinical Work

Certifications & Qualifications

Advanced Degree (MD, DO, PhD, PharmD, or Equivalent)

Industry Keywords

Inflammatory Bowel DiseaseClinical TrialsRegulatory DocumentsCRO ManagementKOL Engagement

About the role

Key responsibilities & impact

Own studies end to end as clinical lead, from protocol through start-up and enrollment
Write protocols and clinical sections of regulatory documents, making study-level design decisions and presenting endpoint, population, and go/no-go recommendations to the Global Program Head
Work with Clinical Operations to hold CROs, sites, and vendors accountable for timelines, enrollment, budget, and data quality
Review blinded safety, PK, and operational data with the medical monitor and act on findings
Work flexibly across decisions and therapeutic indications
Take on studies in additional indications as pipeline needs require
Use AI in daily work to support and improve ways of working, and share effective practices with the team
Build relationships with investigators, sites, and KOLs
Bring the patient's perspective into consequential decisions
Report to the SVP of Clinical Development and collaborate with Global Program Heads, Clinical Operations, and medical monitors

Requirements

What you’ll need

An advanced degree (MD, DO, PhD, PharmD, or equivalent)
Hands-on clinical development experience: written protocols as primary author and taken at least one study from protocol to database lock as its lead
Typically 8+ years for a clinical scientist, or 3+ years in industry after clinical training for a physician
Clinical or trial experience in inflammatory bowel disease, ideally with endoscopic endpoints and central reading (preferred, not required)
Experience in a second therapeutic area
Data-driven judgment using clinical, safety, and operational data to make decisions
Ability or willingness to use AI to draft, check, and interrogate work, with awareness of where it can mislead
Collaborative, direct, high-agency, patient-first approach

Benefits

Comp & perks

Medical, dental, and vision covered at 90%
401(k) with company match
Flexible PTO
Company-wide weeklong recharge break
Adoption assistance