Clinical Manager H/F Position
il y a 4 semaines
Company Overview:
At EndoGene.Bio, we strive to revolutionize women's health by providing high-precision medicine. Our mission is to reduce the time required for endometriosis diagnosis from years to weeks using proprietary biomarkers found in menstrual blood.
We value scientific rigor, daring innovation, and a collaborative work environment. Our team is driven by a passion for making a difference in the lives of patients and healthcare professionals. We believe in empowering our employees to grow and develop their careers, and we offer opportunities for professional development and growth.
Position Overview:
As a Clinical Manager at EndoGene.Bio, you will play a pivotal role in driving our diagnostic solutions to market. This position requires close collaboration with patient advocacy groups, liaising with doctors and hospital teams, developing clinical protocols, and overseeing sample sourcing. Your expertise will contribute directly to the success and growth of our organization.
Key Responsibilities:
Clinical Trials & Protocols:
Develop and write clinical protocols for our diagnostic tests, ensuring adherence to regulatory requirements.
Oversee the execution of clinical studies and trials, monitoring progress and identifying potential risks.
Hospital Recruitment:
Cultivate strong relationships with key opinion leaders, physicians, and hospital administrative staff.
Recruit and onboard hospitals for clinical trials, ensuring they meet all research criteria.
Patient Advocacy Engagement:
Build and maintain relationships with key patient advocacy groups related to endometriosis.
Collaborate with these groups to ensure the patient voice is central in our clinical trials and product development.
Sample Sourcing Activities:
Manage the end-to-end process of sourcing, collecting, storing, and transporting diagnostic samples.
Ensure the highest quality and integrity of samples, adhering to all regulatory and ethical standards.
Team Collaboration:
Work closely with cross-functional teams to ensure alignment on project objectives and deliverables.
Provide periodic updates and presentations to senior management on the progress of clinical projects.
Qualifications:
Medical Doctor (MD) degree, or other degrees + experience in clinical studies in IVD.
Experience in Gynaecology preferred.
Experience in clinical research or clinical project management, preferably related to diagnostics and gynaecological conditions.
Experience working with regulatory guidelines and ethical considerations in in-vitro diagnostic research.
Exceptional interpersonal and communication skills, both written and verbal.
Ability to travel as needed.
Location:
Must be based in France or Spain.
Benefits:
Competitive salary.
Comprehensive health benefits.
Company perks (if on site): transport ticket, meal tickets.
Opportunities for professional development.
Collaborative and innovative work environment.
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