Director – Clinical Development

Codera

Director/Senior Director supporting clinical development strategy and execution for Codera's drug development programs. Collaborating cross-functionally to ensure high-quality clinical data and regulatory compliance.

Posted 6/27/2026full-timeRemote • California • 🇺🇸 United StatesSenior💰 $200,000 - $280,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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The ideal candidate must demonstrate strong expertise in clinical development and regulatory compliance while effectively collaborating across functions to drive clinical trial success. A strategic mindset combined with exceptional communication and problem-solving skills is essential for navigating complex clinical programs.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical DevelopmentClinical Trial ManagementRegulatory ComplianceData AnalysisRisk ManagementProtocol DevelopmentSafety MonitoringClinical Drug DevelopmentClinical Trials OperationsBiometrics Collaboration

Soft Skills

Outstanding Communication SkillsStrategic AgilityCritical ThinkingLogical ThinkingCollaborationDetail-OrientedProblem-SolvingInterpersonal SkillsAdaptabilityTeamwork

Certifications & Qualifications

Bachelor's DegreeAdvanced Degree

Industry Keywords

BiotechnologyPharmaceutical IndustryClinical TrialsHealth AuthoritiesRegulatory AffairsClinical AssetsProgram StrategyCross-Functional CoordinationComplex ProgramsEntrepreneurial Environment

About the role

Key responsibilities & impact

Support the planning and execution of clinical development programs, ensuring alignment with overall program strategy and timelines
Contribute to the evaluation and refinement of development strategies to mitigate risks and advance clinical assets efficiently
Participate in the planning, delivery and cross-functional coordination of clinical trials from early to late phases
Assist in the development, review and refinement of clinical trial protocols, ensuring scientific rigor, ethical conduct and regulatory compliance
Provide medical and clinical input throughout the clinical trial lifecycle, including safety monitoring, data interpretation and risk management
Partner with biometrics and medical writing to ensure clinical and nonclinical studies are designed, analyzed and summarized appropriately in accordance with timelines, good quality practices and applicable regulatory requirements
Collaborate with regulatory affairs and other departments to support regulatory strategies, clinical trial submissions and responses to health authorities
Support data analysis and reporting activities, contributing strategic insights to inform decision-making and regulatory submissions

Requirements

What you’ll need

Bachelor’s Degree required
Advanced degree preferred
Minimum 6 years of clinical development experience within the biotechnology or pharmaceutical industry
Experience with multiple, complex programs or studies
Detailed understanding of end-to-end management of clinical trial conduct, clinical drug development and clinical trials operations
Deep understanding of global regulatory requirements and experience navigating clinical trials to approval
Outstanding written and verbal communication skills, including the ability to use clear language to explain complex ideas
Possess a willingness and ability to work hands-on in a detail-driven, fast-paced, entrepreneurial environment
Strategic agility with strong critical and logical thinking and ability to analyze problems
Ability to establish and maintain collaborative working relationships with internal and external stakeholders

Benefits

Comp & perks

employer sponsored insurance plans including medical, dental and vision coverage
generous paid time off
retirement plan options
additional wellness and professional development programs