Clinical Manager H / F

EndoGene.Bio; Évry; Sur place; EUR 50 000 - 90 000; Plein temps

Résumé du poste

Join a forward-thinking company dedicated to revolutionizing women's health through innovative diagnostic solutions. As a Clinical Manager, you will play a crucial role in developing clinical protocols, managing trials, and collaborating with healthcare professionals to ensure the highest standards of patient care. This is an exciting opportunity to be part of a mission-driven team that values diversity and empowers its members to grow and succeed. If you are passionate about making a difference in women's health and thrive in a collaborative environment, this role is perfect for you.

Prestations

Competitive Salary

Transport Tickets

Meal Tickets

Professional Development Opportunities

Collaborative Work Environment

Qualifications

• Medical Doctor (MD) degree or equivalent with clinical studies experience.
• Experience in Gynaecology preferred.

Responsabilités

• Lead development and writing of clinical protocols for diagnostic tests.
• Build relationships with physicians and hospital staff for clinical trials.

Connaissances

Clinical Research

Project Management

Interpersonal Communication

Regulatory Knowledge

Gynaecology

Formation

Medical Doctor (MD)

Description du poste

At EndoGene.Bio, we aim to bring high-level precision medicine to women’s health. We are working on reducing the diagnosis time for endometriosis from years to weeks through proprietary biomarkers found in menstrual blood.

We believe in doing what is right, not what is easy. We are scientifically driven, daring, and believe that hard work and kindness are unbeatable. When faced with challenges, we collaborate and give our best as a team. We work as a community and strive to empower everyone involved in our journey, from patients to physicians to industry advisors. Our community is our superhero.

We want our team members to grow with us. We value diversity and aim to cultivate a sense of belonging within the company. We encourage you to shape your career by trying new things, shadowing colleagues, and taking courses. Your success is our success.

We are committed to building a legacy in female health, and we want you to be part of our team.

Position Overview :

As a Clinical Manager at EndoGene.Bio, you will play a pivotal role in bringing our diagnostic solutions to market. This role involves collaborating with patient advocacy groups, liaising with doctors and hospital teams, developing clinical protocols, and overseeing sample sourcing. Your expertise will directly contribute to our organization's success and growth.

Key Responsibilities :

1. Clinical Trials & Protocols :
   • Lead the development and writing of clinical protocols for our diagnostic tests.
   • Oversee the execution of clinical studies and trials, ensuring adherence to timelines, budgets, and regulatory standards.
   • Monitor trial progress and identify potential risks, implementing mitigation strategies.
2. Hospital Recruitment :
   • Build strong relationships with key opinion leaders, physicians, and hospital administrative staff.
   • Recruit and onboard hospitals for clinical trials, ensuring they meet research criteria.
   • Provide training and resources to hospital teams involved in our studies.
   • Maintain relationships with patient advocacy groups related to endometriosis, ensuring patient voices are central to our work.
   • Represent the company at advocacy events, conferences, and forums.
3. Sample Sourcing Activities :
   • Manage sourcing, collection, storage, and transportation of diagnostic samples.
   • Maintain high standards of sample quality and integrity, complying with regulatory and ethical standards.
   • Coordinate with labs, storage facilities, and transport providers.
   • Collaborate with R&D, Regulatory, Quality Assurance, and Marketing teams on project goals.
   • Provide updates and presentations to senior management on project progress.

Qualifications :

• Medical Doctor (MD) degree, or equivalent with experience in clinical studies in IVD.
• Experience in Gynaecology is preferred.
• Background in clinical research or project management, especially related to diagnostics and gynecological conditions.
• Knowledge of regulatory guidelines and ethical standards in in-vitro diagnostic research.
• Excellent interpersonal and communication skills, both written and verbal.
• Willingness to travel as needed.
• Languages required: English, French, and Spanish.
• Location: Based in France or Spain.

Benefits :

• Competitive salary.
• Company perks such as transport and meal tickets (if on-site).
• Opportunities for professional development.
• Collaborative and innovative work environment.