Evidence Generation Head

Riyadh - Saudi Arabia

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Job Description Summary

The primary responsibility of this role is to plan develop design and execute Real World Evidence (RWE) studies in Saudi Arabia to develop and demonstrate the value of Novartis marketed and pipeline products to payers and clinicians across different therapeutic areas.

#LI-Onsite

Job Description

Major Accountabilities:

Design and implement innovative Real-World Evidence (RWE) programs to address drug development challenges support regulatory decisions (e.g. label changes new indications) and enable payer decision-making for reimbursement success.

Lead implementation research initiatives including population health models to drive adoption of Novartis innovations aligned with patient and healthcare system needs.

Map and license Real World Data (RWD) sources build research collaborations and execute RWE projects in close partnership with cross-functional teams.

Develop and integrate RWE strategies into product/disease area plans and launch strategies ensuring alignment with global and local evidence plans.

Support integrated evidence planning cost-effectiveness modeling and external HEOR partnerships to strengthen access and reimbursement efforts.

Manage collaborations with investigators KOLs vendors and external stakeholders to co-design innovative study designs and ensure quality delivery of research projects.

Communicate scientifically valid RWE to stakeholders (HCPs payers regulators) and lead internal training on advanced RWE methodologies and implementation science.

Minimum Requirements

A degree as Medical Doctor (MD) or PharmD or PhD. Also if they have a masters degree in health science and/or masters in Evidence Generations / Clinical Research.
Languages:Fluent in English (oral and written) Arabic (native) is preferable.
Minimum 3 years of experience in conducting RWE research for pharmaceutical products within pharma CROs or academic institutions; or in a closely related discipline (e.g. clinical research statistics epidemiology pricing).
Strong understanding of Medical Affairs Drug Development Market Access/HEOR Safety or related areas to generate value evidence from both retrospective and prospective studies.
Good Understanding of Saudi Arabia market research landscape.

Skills Desired

Agility Agility Clinical Practices Cross-Functional Collaboration Data Analysis Drug Development Employee Development Healthcare Sector Understanding Health Sciences Influencing Skills Innovation Inspirational Leadership Integrated Evidence Generation Medical Affairs Medical Communication Medical Education Patient Care People Management Pharmaceutics Priority Disease Areas Expertise Product Launches Product Strategy Real World Evidence (RWE) Regulatory Compliance Research Methodologies 3 more

Job Description SummaryThe primary responsibility of this role is to plan develop design and execute Real World Evidence (RWE) studies in Saudi Arabia to develop and demonstrate the value of Novartis marketed and pipeline products to payers and clinicians across different therapeutic areas.#LI-Onsit...

Job Description Summary

Job Description

Major Accountabilities:

Design and implement innovative Real-World Evidence (RWE) programs to address drug development challenges support regulatory decisions (e.g. label changes new indications) and enable payer decision-making for reimbursement success.

Lead implementation research initiatives including population health models to drive adoption of Novartis innovations aligned with patient and healthcare system needs.

Map and license Real World Data (RWD) sources build research collaborations and execute RWE projects in close partnership with cross-functional teams.

Develop and integrate RWE strategies into product/disease area plans and launch strategies ensuring alignment with global and local evidence plans.

Support integrated evidence planning cost-effectiveness modeling and external HEOR partnerships to strengthen access and reimbursement efforts.

Manage collaborations with investigators KOLs vendors and external stakeholders to co-design innovative study designs and ensure quality delivery of research projects.

Communicate scientifically valid RWE to stakeholders (HCPs payers regulators) and lead internal training on advanced RWE methodologies and implementation science.

Minimum Requirements

A degree as Medical Doctor (MD) or PharmD or PhD. Also if they have a masters degree in health science and/or masters in Evidence Generations / Clinical Research.
Languages:Fluent in English (oral and written) Arabic (native) is preferable.
Minimum 3 years of experience in conducting RWE research for pharmaceutical products within pharma CROs or academic institutions; or in a closely related discipline (e.g. clinical research statistics epidemiology pricing).
Strong understanding of Medical Affairs Drug Development Market Access/HEOR Safety or related areas to generate value evidence from both retrospective and prospective studies.
Good Understanding of Saudi Arabia market research landscape.