20 beste Stellen als regulatory in bâle bs – aktuell auf Personalsuche

Senior HEOR Manager Patient-Reported Outcome (12 months contract) m/f/d
Bayer —Basel, BS
- Doktorat
- Forschungserfahrung
- Master
3 Tage
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Monte Rosa Therapeutics, Inc —Basel, BS
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IQVIA —Basel, BS
- 100%
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- Englisch
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Ridgeline Discovery —Basel, BS
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Direkt bewerben
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Swiss Biotech Association —Basel, BS
- Doktorat
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1 Tag

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

Bayer -
Basel, BS

Jetzt bewerben

Details zur Stelle

Befristet
vor 3 Tagen

Qualifikationen

Doktorat
Forschungserfahrung
Master
Führungserfahrung

Vollständige Stellenbeschreibung

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.

We are looking forward to receiving your application by 15th June. Thank you!

#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

Jetzt bewerben

Erweiterte Suche

regulatory Jobs in bâle bs

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

Expert Imaging Lead, CVRM

Senior Coordinator Distribution Europe

Global Medical Director

Senior Manager - Post-Market Clinical Follow-up

Associate Director - HNC Regional Science EMEA

Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge

Director / Associate Director – Toxicology

Senior Statistical Methodology Data Scientist

(Sr.) Site Activation Specialist (m/w/d), office-based in Basel, Switzerland

Associate Director Quality - Client Dedicated Process & QD Manager (m/w/d)

Director, Clinical Development

Director, Business Relationship Management — Commercial, Digital, Data & AI

Head Banking Products & Product Governance

Quality Engineer Compliance 80-100% (f/m/d)

Principal Scientist - Pharma Biosample Services (PBS) Lab Head Basel

Investment Specialist (w/m/d) Parttime/Fulltime

Data Scientist (Translational Data, Transfers & Statistics – Phase I)

Student Internship in Order and Distribution Management (w/m/d, starting July 2026, up to 12 Months)

Director, Toxicology

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