Director Real World Evidence

Barrington James; Massachusetts; On-site; USD 180,000 - 240,000; Full time

Job summary

Barrington James is seeking a Director, Real World Evidence to own the RWE strategy for a high priority development program. This senior IC role works across clinical development, regulatory, medical affairs and market access.

The position requires 6+ years in RWE/epidemiology, oncology experience preferred, and a strong track record in managing observational studies and data sources. Join a global biopharma client and drive strategic evidence planning.

Qualifications

• 6+ years in RWE, epidemiology or pharmacoepidemiology.
• Pharmaceutical, biotechnology or CRO experience.
• Product level RWE strategy ownership.
• Strong claims, EHR/EMR and registry study experience.
• Oncology experience strongly preferred.
• Master's or PhD in epidemiology, public health, HEOR, biostatistics or a related field.

Responsibilities

• Own program level RWE strategy and integrated evidence planning.
• Lead observational and non interventional studies from protocol through reporting.
• Identify and select claims, EHR and registry data sources.
• Support regulatory submissions and Health Authority interactions.
• Manage CROs, vendors, study budgets and timelines.
• Lead publications and represent the company externally.

Skills

RWE strategy

EHR data

Observational studies

Regulatory submissions

Vendor management

Education

Master's or PhD in epidemiology/HEOR

Job description

Our client, a global biopharma is hiring a Director, Real World Evidence to own RWE strategy for a high priority development program.

This is a senior IC position working across clinical development, regulatory, medical affairs and market access.

Responsibilities

• Own program level RWE strategy and integrated evidence planning.
• Lead observational and non interventional studies from protocol through reporting.
• Identify and select claims, EHR and registry data sources.
• Support regulatory submissions and Health Authority interactions.
• Manage CROs, vendors, study budgets and timelines.
• Lead publications and represent the company externally.

Required Skills

• 6+ years in RWE, epidemiology or pharmacoepidemiology.
• Pharmaceutical, biotechnology or CRO experience.
• Product level RWE strategy ownership.
• Strong claims, EHR/EMR and registry study experience.
• Oncology experience strongly preferred.
• Master's or PhD in epidemiology, public health, HEOR, biostatistics or a related field.