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The Medical Science Liaison serves as the primary scientific interface between the company and healthcare professionals, facilitating scientific exchange and gathering field insights. They also support evidence generation, clinical trial feasibility, and cross-functional strategic initiatives across the Nordic region.
The Senior Medical Director provides medical oversight and monitoring for oncology and hematology clinical trials while ensuring scientific credibility and regulatory compliance. They also partner with business development to support growth through bid strategy, proposals, and building relationships with key opinion leaders.
The specialist will manage account profiling and develop relationships with key healthcare stakeholders to drive procalcitonin testing strategies. They are responsible for delivering clinical education programs and meeting annual operating growth targets within their designated region.
The Global Medical Education Manager develops and executes comprehensive internal and external educational programs to support the safe and effective use of Getinge products. This role involves coordinating with cross-functional teams, engaging with healthcare professionals, and managing global medical education initiatives.
The manager is responsible for driving lifecycle value across the installed base through automation modernization initiatives and care agreements. They will lead the evolution of the service portfolio while ensuring cross-functional alignment and measurable business impact.
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The Director will lead the global medical affairs strategy for the Heart Failure division, overseeing clinical research, product safety, and scientific engagement. They will collaborate cross-functionally to support clinical trials, regulatory interactions, and professional education initiatives to advance heart failure therapies.
The Principal Biostatistician serves as the statistical lead for late-phase clinical trials, providing scientific oversight and strategic guidance. They are responsible for authoring statistical analysis plans, performing complex analyses, and representing the biostatistics function within cross-functional clinical teams.
The Medical Director provides medical leadership for clinical trials, including protocol development, medical monitoring, and safety evaluation. They serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and effective issue resolution.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects. They will also provide central monitoring by reviewing neuropsychological test data to ensure accuracy and provide feedback to other raters.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects and caregivers. They will also provide central monitoring by reviewing test data to ensure accuracy and providing feedback to other raters.
The role involves conducting patient interviews and clinical assessments while ensuring the integrity and reliability of clinical trial data. The rater will provide guidance to other raters on methodology and scoring techniques through live interactions.
Perform manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles will also participate in clinical decision-making and oversee site-facing interventions and rater remediation.
You will be responsible for building relationships with healthcare professionals in hospitals to drive product adoption and improve patient access in the diabetes sector. Additionally, you will lead the planning and execution of nationwide field events and collaborate with internal teams to optimize sales strategies.
The role involves shaping and executing medical and business strategies for the cardiorenal therapy area while building scientific partnerships with healthcare professionals. You will translate scientific insights into strategic actions and support evidence generation, clinical development, and lifecycle activities.
You will provide critical diagnostic information for veterinary patients while receiving mentorship and feedback from experienced radiologists. The role involves reading both known and live cases to prepare for board certification and maintain high reporting standards.
The CRA is responsible for managing the full lifecycle of study sites, including qualification, initiation, monitoring, and close-out. They ensure protocol adherence, verify source documents for data veracity, and provide guidance to site staff and junior CRAs.
The role involves locating individuals or companies within a geographic area to deliver legal documents against a receipt. Reporting is handled via a web-based data system, with work primarily performed during evenings and weekends.
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Provide high-quality mental health support through psychotherapy, counseling, or coaching sessions. Lead support groups and deliver Masterclasses to clients across the Asia-Pacific region and Europe.
Conduct 45-minute online psychological counseling sessions to help clients improve their mental well-being. Identify client needs and provide individualized, sustainable solutions for issues ranging from stress to career growth.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
Coordinates and facilitates clinical trial activities, providing administrative and technical support to the project team. Manages study documentation, performs file reviews, and acts as a liaison for cross-functional project initiatives.
The Clinical Assessment Scientist will act as a COA Lead, collaborating with cross-functional teams to deliver clinical solutions for drug development projects. They will apply therapeutic expertise to understand customer needs and drive progress across the drug development continuum.
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