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Verto People Ltd in the United States is seeking a Vice President of Clinical Development for Immunology/Biologics. You will lead global early-stage programs from candidate selection through FIH and Phase 2a PoC, shaping clinical strategy and cross-functional execution.
The ideal candidate holds an MD or MD-PhD, 7–10+ years in biotech/pharma, with strong immunology and biologics experience, and a track record of regulatory success and leadership.
Location: United States | Remote
Employment: Full-Time | Permanent
Level: Vice President
Therapeutic Area: Immunology / Immune-Mediated Diseases
Are you an experienced Clinical Development leader with a strong background in immunology and early-stage drug development? This is an exciting opportunity to join an innovative, rapidly growing biotechnology company leveraging AI-driven drug discovery and next-generation biologics to develop breakthrough therapies for patients with immune-mediated diseases.
We are seeking a strategic, hands-on VP of Clinical Development to lead global clinical development programmes from candidate selection and IND-enabling activities through First-in-Human (FIH), Phase 1, Phase 1b and Phase 2a Proof-of-Concept (PoC) studies. The successful candidate will thrive in a fast-paced biotech environment, combining strong medical and scientific judgement with the ability to lead cross-functional teams, shape clinical strategy and drive critical development decisions.
Key Responsibilities:
Define and lead global clinical development strategies across early-stage immunology programmes, from preclinical development through Phase 2a Proof-of-Concept.
Oversee clinical trial design, protocol development, medical monitoring, safety assessments and clinical data interpretation.
Lead critical decisions relating to dose selection, patient populations, study endpoints, biomarkers and indication strategy.
Provide scientific leadership, guidance and mentorship to Clinical Leads and Clinical Scientists.
Lead the transition of preclinical candidates into clinical development, including IND/CTA readiness and First-in-Human studies.
Partner closely with Clinical Operations to oversee CROs, external vendors, trial timelines, budgets and study delivery.
Collaborate with Regulatory Affairs, Translational Medicine, Clinical Pharmacology, CMC, Safety and Research teams to ensure integrated development strategies.
Lead interactions with regulatory authorities, key opinion leaders and external development partners.
Identify clinical, scientific and regulatory risks, implementing effective mitigation strategies.
Present clinical development strategies, programme updates and investment recommendations to executive leadership.
Candidate Requirements:
MD or MD-PhD qualification - essential.
7-10+ years of clinical development experience within the biotechnology or pharmaceutical industry.
Strong experience in immunology or immune-mediated diseases, including dermatology, rheumatology, gastroenterology or respiratory indications.
Proven experience leading global early-phase clinical development programmes, particularly FIH, Phase 1 and Phase 2a PoC studies.
Experience developing biologics, monoclonal antibodies, multispecific antibodies or other innovative therapeutic modalities.
Strong understanding of IND/CTA submissions, clinical trial design, regulatory requirements and clinical safety monitoring.
Demonstrated experience leading cross-functional clinical development teams and managing external CROs and vendors.
Ability to interpret emerging clinical and translational data to guide development strategy and decision-making.
Excellent strategic leadership, communication and stakeholder management skills.
Comfortable working in a fast-paced, entrepreneurial biotechnology environment.
What's on Offer?
Senior executive leadership opportunity within an innovative, rapidly growing biotechnology company.
Opportunity to shape the clinical development strategy for a pipeline of next-generation immunology therapies.
Exposure to cutting-edge AI-enabled drug discovery and biologics development.
Significant influence over clinical programmes, portfolio decisions and future development strategy.
Opportunity to lead global clinical development programmes from preclinical stages through clinical Proof-of-Concept and beyond.
Collaborative, science-driven environment with direct exposure to executive leadership and strategic development partners.