As a Clinical Research professional, you will direct clinical studies to ensure projects are appropriately resourced and staff are trained, and project objectives are met.  You will work with senior leadership in formulating effective strategic goals and objectives for designated team and clients and ensure operational alignment with organization priorities.

• Design and execute Phase-2b and Phase-3 clinical trials and large non-interventional studies (NIS)
• Develop research study documents and trial SOPs, aligned with GCP/ICH guidelines and other applicable regulations
• Develop and maintain procedures for regulatory reporting and compliance
• Manage CTMS and EDC platforms
• Create research reports and other documents in PPT and MS Word formats
• Conduct literature reviews on various scientific topics
• Create abstracts, posters, manuscripts
• Engage and communicate effectively with internal and external stakeholders
• Create abstracts, posters, manuscripts

• A degree in life sciences, nursing or medicine
• A minimum of 5 years of prior clinical trial leadership experience, ideally in a full-service CRO setting
• Global Phase-2b/Phase-3 trial experience
• Knowledge of GCP, ICH guidelines and regulatory (FDA/EMA) requirements for clinical trial management
• Knowledge of regulatory (FDA/EMA) reporting and compliance requirements
• Hands-on experience in managing CTMS and EDC portals
• Proficient in project management skills
• Strong technical writing skills, and communication skills
• Familiar with scientific literature search/evaluations
• Native-level proficiency in Spanish, French or German (optional)

If you are interested in exploring this opportunity with Avant Health, please submit your CV and a cover letter (stating your research interests, academic qualifications, past relevant experience, and salary expectations) to Info@Avant-Health.com.