In-House CRA

Posted 23 Days Ago
Be an Early Applicant
Berlin
Mid level
Healthtech • Pharmaceutical
The Role
Responsible for supporting clinical research activities, ensuring adherence to protocols, and assisting in monitoring, reporting, and training for clinical studies.
Summary Generated by Built In

Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

How you will make an impact:

You will be responsible for remotely supporting field clinical research associate/ site activities to ensure the overall integrity of study implementation and adherence to study protocol at assigned clinical sites.
Key Responsibilities:

  • Organizing and supervising clinical study:

  • Assist and conduct Clinical Monitoring activities

  • 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'll need (Required):

Education and Experience:
Bachelor's Degree in in related field , 3 years years experience of previous related medical device and/or clinical experience Required or
Associate's Degree or equivalent in in related field , 5 years years experience of previous field monitoring experience, quality assurance/control and regulatory compliance Required
 

What else we look for (Preferred):

Additional Skills:
• 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
 

What is  it  like  to work at  Edwards  Lifesciences  in  Germany?

As a global leader in patient-focused medical innovations, we offer rewarding opportunities and exciting challenges in a truly international, dynamic and friendly work environment.

We are committed to fostering a diverse and inclusive work environment where all employees can grow, personally and professionally. To achieve this, we offer on-the-job development, training opportunities and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).  

Edwards  Lifesciences  in  Germany  also  offers  the  following  benefits:

  • Competitive  Compensation  and  Benefits  package

  • Flexible  working  hours,  remote  working

  • Pension  plan Risk  

  • Insurance Meal  Benefits  

  • Service  Awards Enhanced  

  • Leave  Benefits

  • Transportation  Benefits

  • Employee  Stock  Purchase  Program

  • Employee  Assistance  Program

  • Comprehensive Wellness  Program  including  onsite  gym,  yoga classes  and  massage,  preventive health  checks,  healthy  lifestyle  webinars,  educational events,  charity  activities  and  much  more.

Benefits  are  regulated  by  an  internal policy  which  contains  the full  details regarding  the entitlement and  conditions  for  the  benefits.  Benefits  policy and  components  may  vary  by  location. 

Top Skills

Ms Office Suite
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The Company
Draper, Utah
13,687 Employees
On-site Workplace
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more.

Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today.

Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives.

Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life.

For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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