How you will make an impact:

• Conducting Clinical Monitoring activities at sites across Germany
• Serve as key contact to assigned clinical sites throughout the study process
• Is accountable for achieving and reporting on agreed clinical milestones
• Supports study team in the interactions with Ethics Committees and Competent Authorities
• Participates actively to project team meetings, as required
• Close collaboration with internal stakeholders to ensure proper project conduct
• Assist in Providing site and Edwards personnel training including preparation/maintenance of study documents, completion of forms, understanding of examinations/assessments required
• Reporting site enrollment progress including device accountability and protocol deviations (inclusion/exclusion criteria, sequential enrollment) 6. Collecting completed Case Report Forms (CRF) and collecting, confirming and auditing supporting documentation.
• Processing adverse events
• Document procedural case observations for insights in investigating post procedural events
• Data review, safety reporting and complaint handling
• Identifying and reporting adverse events and device-related complications in accordance with regulatory and internal requirements
• Develop new improved processes and perform implementation
• Ensures Audit readiness for internal, external and site Audits
• Other incidental duties as assigned by management

What you will need (required):

• Bachelor's Degree in a related field, and/or proven record of strong relevant experience.
• Previous related medical device and/or clinical experience required
• Previous clinical trial site monitoring experience in Germany within a Medical Device or Pharmaceutical setting.
• Experience of different types of monitoring visits and in different study stages.
• Quality assurance and regulatory compliance in a clinical research setting
• Driving licence required
• Fluency in both English and local language (French or German as applicable) is essential.

What else we look for (preferred):

• Excellent communication and organizational skills
• Proven expertise in MS Office Suite and ability to operate general office machinery
• Good written and verbal communication skills, presentation, and interpersonal relationship skills including negotiating and relationship management skills
• Good problem-solving and critical thinking skills
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
• Cardiology and/or medical device study experience desirable.

How you will make an impact:

• Conducting Clinical Monitoring activities at sites across Germany
• Serve as key contact to assigned clinical sites throughout the study process
• Is accountable for achieving and reporting on agreed clinical milestones
• Supports study team in the interactions with Ethics Committees and Competent Authorities
• Participates actively to project team meetings, as required
• Close collaboration with internal stakeholders to ensure proper project conduct
• Assist in Providing site and Edwards personnel training including preparation/maintenance of study documents, completion of forms, understanding of examinations/assessments required
• Reporting site enrollment progress including device accountability and protocol deviations (inclusion/exclusion criteria, sequential enrollment) 6. Collecting completed Case Report Forms (CRF) and collecting, confirming and auditing supporting documentation.
• Processing adverse events
• Document procedural case observations for insights in investigating post procedural events
• Data review, safety reporting and complaint handling
• Identifying and reporting adverse events and device-related complications in accordance with regulatory and internal requirements
• Develop new improved processes and perform implementation
• Ensures Audit readiness for internal, external and site Audits
• Other incidental duties as assigned by management

What you will need (required):

• Bachelor's Degree in a related field, and/or proven record of strong relevant experience.
• Previous related medical device and/or clinical experience required
• Previous clinical trial site monitoring experience in Germany within a Medical Device or Pharmaceutical setting.
• Experience of different types of monitoring visits and in different study stages.
• Quality assurance and regulatory compliance in a clinical research setting
• Driving licence required
• Fluency in both English and local language (French or German as applicable) is essential.

What else we look for (preferred):

• Excellent communication and organizational skills
• Proven expertise in MS Office Suite and ability to operate general office machinery
• Good written and verbal communication skills, presentation, and interpersonal relationship skills including negotiating and relationship management skills
• Good problem-solving and critical thinking skills
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
• Cardiology and/or medical device study experience desirable.