Clinical Research Director - Immunology

Excelya is seeking a Clinical Research Director (CRD) in Immunology, a physician‑scientist responsible for providing medical leadership and scientific oversight across clinical development programs in immunology.

The Clinical Research Director acts as the medical reference for assigned clinical trials, ensuring scientific quality, patient safety, regulatory compliance, and cross‑functional alignment throughout the clinical development lifecycle.

Main Responsibilities

• Lead the medical and scientific oversight of clinical trials in immunology across development phases
• Author, review, and approve key clinical documents including abbreviated protocols, clinical protocols, informed consent forms (ICF), and related protocol/ICF amendments
• Provide medical support for study feasibility assessments and real‑world data evaluations relevant to clinical development
• Contribute to responses to Health Authorities (HAs) , Ethics Committees (ECs) , clinical sites, and global/local study teams
• Participate in, prepare for, and contribute to investigator meetings, monitoring meetings, and cross‑functional project meetings
• Establish, manage, and provide ongoing oversight of expert committees, including Steering Committees , Data Monitoring Committees (DMCs) , and Adjudication Committees , covering member selection, charter development, meeting coordination, reporting, and documentation
• Provide medical guidance, training, and support to internal teams (Clinical Study Operations, Global Study Managers, biostatistics, Medical Affairs, Clinical Project Leaders), CROs, and investigators
• Provide medical input into study plans, including Clinical Monitoring Plans (CMP), Medical Review Plans (MRP), Data Review & Data Surveillance strategies (DR & DS), Safety Risk Management Plans (SRMP), CRFs, CRF completion guidelines, and deviation management
• Support data review activities, statistical surveillance, medical coding, medical validation, and development of clinical case review materials
• Perform clinical case reviews including patient profile assessments and review/validation of narratives
• Review and endorse Statistical Analysis Plans (SAPs)
• Contribute to the preparation of key study deliverables, including Clinical Study Reports (CSR) and review of scientific publications
• Prepare for and respond to audits and regulatory inspections related to clinical development activities

Requirements

About You:

• Experience: Medical Doctor (MD) with proven expertise in immunology and clinical research
• Strong experience in clinical development and medical leadership roles
• Education: Medical Doctor (MD) or Clinical Physician degree required; additional certifications in clinical research or project management are a plus
• Skills: In-depth knowledge of immunology clinical trials, regulatory environments, and GCP standards; excellent leadership, communication, and organizational abilities
• Languages: Fluent in English and French is preferred