Senior Clinical Research Manager; REMOTE

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

The Senior Manager, Clinical Research is responsible for the planning, execution and interpretation of clinical trials and registries at Varian, as well as managing several Clinical Trial Managers. This person will ensure adherence with internal procedures and external clinical trial requirements, as well as ensuring projects are appropriately resourced and employees are trained and meeting project objectives.

• Accountable for the delivery of studies or programs that are critical to a product’s clinical development, ensuring that they are completed on time, within budget and in compliance with SOPs, regulations and ICH/GCP guidelines
• Performs all required management responsibilities including but not limited to: implementing the company's policies, programs, and guidelines; ensuring employee productivity and growth; managing resources; knowing Varian's business; and maintaining functional, technical, and external market awareness necessary for managing immediate organization.
• Communicate study status, cost and issues to ensure timely decision-making by senior management
• Initiate and manage study-level timelines, including communication to internal and external team members on deliverables
• Oversee the creation of site materials including training, manuals and support documentation
• Perform periodic review of clinical data, quality metrics and study deviations
• Develop timelines and budgets for assigned studies/programs and is responsible for delivery to both quality and agreed timelines.
• Develop and implement robust contingency and issue management plans to solve complex issues that impact study or program milestones.
• Provides input into the development of study protocols and CRFs to ensure studies are designed and planned to be achievable

• Bachelor's degree in related field; minimum of 6 years of clinical operations experience in industry or CRO setting
• 3+ years of management experience
• Exceptional communication and interpersonal skills
• Excellent written and oral communication skills
• Knowledge of national / regional clinical trial regulations and industry standards regarding interactions with healthcare professionals essential
• Wide-ranging experience, uses professional concepts and company objectives to resolve complex issues in creative and effective ways

We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare.

For everyone. Everywhere. Sustainably.

$161,170 - $221,606

Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.

The Company offers the following benefits for this position, subject to applicable eligibility requirements:…