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PATIENT-CENTERED OUTCOMES RESEARCH (P-COR) LEAD

Barcelona - Barcelona

Descripción de la oferta de empleo

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.
Patient-Centered Outcomes Research (P-COR) Lead     Position purpose (A brief statement indicating the basic purpose of the position).
  The P-COR Lead is responsible for clinical outcome assessment (COA) related activities and projects across any therapeutic area within the organization, with a strong ‘patient-first’ mindset.
The role is reliant on a capability for COA strategic planning and thinking, high impact and impeccable scientific integrity.
This position involves collaboration and leadership with internal cross-functional teams and external vendors to ensure the successful implementation and completion of COA initiatives, including patient- reported outcomes (PROs), clinician-reported outcomes (ClinROs), and other COA assessments for clinical programs.
The purpose of the position is to maximize opportunities to enhance the patient experience, from trial design to final reporting.
While leading COA related project activities, the incumbent uses his/her expertise and insights to inform patient-centered clinical design and further leads the identification of concrete additional regulatory or market access requirements that might be needed within a clinical program (e.
., COA validation activities outside the trial, exit interviews).
The ultimate end goal is to result in commercial and regulatory success of products that include COAs in their endpoint measurement strategy across clinical lifecycles.
  Scope.
Global   Major tasks and responsibilities of position.
  Lead the development, creation and execution of strategic clinical outcome assessment (COA) plans for products in all therapeutic area across the company.
Guide internal teams for clinical programs in choosing the appropriate COAs for clinical trials and provide input into the majority of clinical documents as needed, throughout the clinical trial lifecycle (e.
., protocols, statistical or psychometric analysis plans, results, and/or clinical reports).
Lead the scientific execution of COA projects from start to finish with outside vendors and internal stakeholders (i.
.
P-COR Project Manager, clinical, medical affairs, market access, regulatory, and commercial teams or beyond).
Provide guidance and direction to project teams, ensuring adherence to COA specific regulatory requirements, best practices and industry standards related to COAs, including advising the scientific rigor for translation, cultural adaptation and electronic COA implementation activities within trials.
Oversee and own COA content validation and psychometric validation activities, analyses and outputs.
Work with biostatisticians/psychometricians, clinical and data management teams to interpret and report COA data and prepare and submit regulatory or scientific documents as needed (e.
.
FDA or EMA dossiers, briefing books, and manuscripts).
Lead in preparing relevant sections of meetings, documentation and communication for regulatory agencies (Type C meetings, dossiers and briefing books) or manuscripts in support of communication and commercial product goals with other cross-functional teams (e.
., regulatory, clinical teams, and medical writing).
Stay up to date with COA related leading scientific organizations and bodies (e.
.
C-Path Institute, PCORI, ISPOR, ISOQOL etc.) and recent methodologies or latest hot topics.
   what are the main objectives of the function?   This role will be key to ensure Bayer’s clinical programs and products are strategically informed by, and centered around a rigorous COA strategy and patient-centered approach, directly influencing the commercial success of products.
    Work relations.
Internal.
P-COR Project Manager, on a regular basis Clinical, Medical Affairs, Regulatory, Commercial, Digital Health and more closely, with Market Access Leads throughout COA project lifecycles Product Teams (PTs) during COA related touchpoints and needs for specific program The CD&PE and CCC team members and other project scientific related nuclei External.
Outsourcing partners/vendors Clinical experts Patient advocacy organizations or beyond     Qualifications (Education, skills, experiences and personal characteristics necessary for success in this position) Education.
At least a master’s degree in Life Sciences, Psychology, Sociology, Psychometrics, Pharmacy, Biostatistics, or a related field.
Ph.
.
is preferred.
Experience.
Minimum of 5 years of applied experience and leadership in health outcomes research, ideally in the COA/PRO area.
In-depth knowledge of COA methodologies and regulatory requirements.
Analytics.
Strong ability to understand and analyze COA data, apply COA validation methodologies (e.
., translation and linguistic validation) and output for qualitative and quantitative COA research methods to derive rigorous regulatory ready insights Strategy.
Strong ability to develop strategies and implement tactics for optimal clinical outcome strategy, to address any market access or regulatory needs globally Leadership.
Excellent leadership and communication skills, collaboration and communication skills to ensure implementation of COA strategies in for all nuclei Digital.
Understanding of electronic COA migrations from paper, BYOD and/or latest eCOA implementation standards Interaction.
Proven experience in successfully interacting with multiple stakeholders internally and externally, while leading COA activities within cross-functional teams with strong problem-solving skills External collaboration.
High degree of empathy and inclusive mindset to work with diverse external stakeholder groups Strong ability to self-organize.
Collaborate effectively without hierarchical authority and with accountability, pro-active and inclusive mindset, strong display of DSO behaviors WHAT WE OFFER   Guided by our mission  “Health for all, Hunger for none”,  we deliver breakthrough innovations in healthcare and agriculture.
If you’re looking to build a meaningful career in a community of creative and diverse people dedicated to making a difference, join us!   We offer you:    Flexible & hybrid work model.
Career development & learning opportunities.
Work-life balance for your physical & mental wellbeing.
Competitive salaries & financial wellbeing (e.
.
life insurance).
We promote employee's well-being, Inclusion & diversity and sustainability in a collaborative and innovative environment.
We promote social engagement through our volunteering program.
YOUR APPLICATION       This is your opportunity to tackle the world’s biggest challenges with us.
Maintaining our health, feeding growing populations and slowing the rate of climate change.
You have a voice, ideas and perspectives and we want to hear them.
Because our success begins with you.
Be part of something big.
Be Bayer.
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.
Location.
Spain.
Cataluña.
Barcelona      Division.
Enabling Functions     Reference Code.
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Detalles de la oferta

Empresa
  • Sin especificar
Localidad
Dirección
  • Sin especificar - Sin especificar
Tipo de Contrato
  • Sin especificar
Fecha de publicación
  • 24/09/2024
Fecha de expiración
  • 23/12/2024
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