Senior HEOR Manager Patient-Reported Outcome (12 months contract) m/f/d

Bayer CropScience Limited; Basel; Vor Ort; CHF 140.000 - 190.000; Vollzeit

Zusammenfassung

Bayer is seeking a Senior HEOR Manager for Patient-Reported Outcomes on a 12-month contract in Basel. You will lead COA strategy, guide trial planning, and manage external vendors to ensure regulatory-ready COA data across programs.

The role demands 5+ years in health outcomes research, strong COA/PRO expertise, and experience navigating regulatory and HTA environments. Collaboration with multiple teams and stakeholders is essential.

Qualifikationen

• A master's or PhD in Life Sciences or related fields is required or preferred.
• Minimum 5+ years in health outcomes research with COA/PRO expertise.
• Experience leading cross-functional teams and external vendors.
• Strong understanding of COA regulatory and HTA requirements.
• Knowledge of electronic COA migrations and modern COA standards.

Aufgaben

• Lead development and execution of strategic COA plans across programs.
• Guide teams in selecting COAs for clinical trials and documents.
• Lead scientific COA projects with vendors and stakeholders.
• Ensure COA regulatory requirements and best practices are followed.
• Oversee COA validation and interpretation with psychometric evidence.
• Collaborate on COA data analysis and regulatory submissions as needed.
• Stay current with COA science and integrate advances into programs.

Kenntnisse

COA/PRO methodology

COA data analysis

Regulatory and HTA compliance

Cross-functional leadership

Vendor management

Trial design input

Stakeholder communication

Ausbildung

Master’s degree in Life Sciences, Psychology, Sociology, Psychometrics, Pharmacy, Biostatistics, or related field

Ph.D. preferred

Tools

eCOA implementation standards

Jobbeschreibung

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Senior HEOR Manager Patient-Reported Outcome (12 months contract) m/f/d

As a Senior HEOR Manager COAs/PROs, you are at the forefront of clinical outcome assessment (COA) activities and projects across various therapeutic areas within our organization, always prioritizing a 'patient-first' mindset. Your role is pivotal in COA strategic planning and execution, ensuring high impact and scientific integrity. You will collaborate and lead internal cross-functional teams and external vendors to successfully implement COA initiatives, including patient-reported outcomes (PROs), clinician-reported outcomes (ClinROs), and other COA assessments for clinical programs. Your mission is to enhance the patient experience from trial design to final reporting, ensuring commercial and regulatory success of products that include COAs in their endpoint measurement strategy across clinical lifecycles.

YOUR TASKS AND RESPONSIBILITIES:

• Lead the development and execution of strategic COA plans for products across therapeutic areas, owning the COA Strategy Document for each program;
• Guide internal teams in selecting appropriate COAs for clinical trials and provide input into clinical documents throughout the trial lifecycle;
• Lead the scientific execution of COA projects with external vendors and internal stakeholders;
• Provide guidance to project teams, ensuring adherence to COA regulatory requirements and best practices;
• Oversee COA validation and interpretation, ensuring psychometric evidence meets regulatory and HTA criteria;
• Collaborate on COA data analysis and reporting, preparing regulatory or scientific documents as needed;
• Prepare COA-related regulatory and scientific submissions, leading relevant sections for regulatory agencies;
• Stay current with COA-related scientific organizations and methodologies, incorporating advances into programs.

WHO YOU ARE:

• At least a master’s degree in Life Sciences, Psychology, Sociology, Psychometrics, Pharmacy, Biostatistics, or a related field. A Ph.D. is preferred;
• 5+ years of applied experience in health outcomes research, with demonstrated leadership and expertise in COA/PRO methodology and regulatory requirements;
• Strong ability to analyze and validate COA data, apply COA validation methodologies, and derive regulatory-ready insights;
• Ability to develop strategies and implement tactics for optimal clinical outcome strategy addressing market access or regulatory needs globally;
• Excellent leadership skills with experience leading cross-functional teams and managing external vendors;
• Understanding of electronic COA migrations and latest eCOA implementation standards;
• Proven ability to interact effectively with internal and external stakeholders, navigating competing priorities;
• High degree of empathy and inclusive mindset to work with diverse external stakeholder groups.

#LI-CH

YOUR APPLICATION

Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.

Bayer is committed to providing barrier-free access and support-facilities for individuals with disabilities - during the application process and beyond. Applicants with disabilities are encouraged to request any support / equipment they may need via the contact information below.

Location: Switzerland : Basel-City : Basel

Division: Pharmaceuticals

Reference Code: 872341