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Director Real World Evidence Rwe Jobs in Racine, WI

Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g ...

Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g ...

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Director Real World Evidence Rwe information

What is the difference between Director Real World Evidence Rwe vs Clinical Data Manager?

AspectDirector Real World Evidence RweClinical Data Manager
CredentialsAdvanced degrees (PhD, MD, or Master’s), industry certificationsBachelor’s or Master’s in life sciences, clinical research
Work EnvironmentStrategic, cross-functional teams, senior managementData collection, database management, clinical trial sites
Industry UsagePharmaceuticals, biotech, healthcare analyticsClinical research organizations, pharmaceutical companies

The main difference is that the Director Real World Evidence Rwe focuses on designing and leading real-world data studies to inform healthcare decisions, while the Clinical Data Manager handles the collection and management of clinical trial data. The Rwe director has a broader strategic role, whereas the Clinical Data Manager is more operational and detail-oriented.

Who is the director of R&D?

The Director of R&D (Research and Development) is responsible for overseeing the development of new products, innovations, and research strategies within an organization. This role typically requires strong leadership, scientific expertise, and project management skills to guide research teams and ensure project milestones are met.

What does a director of clinical informatics do?

A director of clinical informatics oversees the implementation and management of healthcare information systems to improve patient care and operational efficiency. They coordinate between IT teams, clinicians, and administrators, often utilizing electronic health records (EHR) and data analytics tools to optimize clinical workflows and ensure data security.

What does a director of product innovation do?

A director of product innovation oversees the development and implementation of new products or features, driving growth and competitive advantage. They collaborate with cross-functional teams, analyze market trends, and utilize project management skills to bring innovative ideas to market efficiently.

What is RWE real world evidence?

Real World Evidence (RWE) is data collected from real-world settings such as electronic health records, claims data, and patient registries. In the context of a Director of Real World Evidence, it involves analyzing this data to support healthcare decision-making, regulatory submissions, and clinical research. Skills in data analytics, biostatistics, and familiarity with healthcare data sources are essential for this role.
What are the most commonly searched types of Real World Evidence Rwe jobs in Racine, WI? The most popular types of Real World Evidence Rwe jobs in Racine, WI are:
What are popular job titles related to Director Real World Evidence Rwe jobs in Racine, WI? For Director Real World Evidence Rwe jobs in Racine, WI, the most frequently searched job titles are:
What job categories do people searching Director Real World Evidence Rwe jobs in Racine, WI look for? The top searched job categories for Director Real World Evidence Rwe jobs in Racine, WI are:
Medical Science Liaison. Great Lakes

Medical Science Liaison. Great Lakes

UCB

Milwaukee, WI

$134K - $204K/yr

Other

Posted 29 days ago


Job description

Make your mark for patients

UCB is looking for an experienced, science-driven and patient-focused Medical Science Liaison (MSL) to work on the Epilepsy & Rare Syndromes team for the Great Lakes geography that includes Michigan, Wisconsin, Minnesota and North Dakota.

About the role
The Medical Science Liaison (MSL), Great Lakes, will engage with key scientific and medical influencers to advance understanding of UCB's Epilepsy and Rare Syndromes portfolio. This role fosters collaborative, science-driven partnerships with key stakeholders to support optimized patient care. The MSL will provide scientific exchange, contribute insights to medical strategies, and drive patient-focused initiatives within the local health ecosystem.
What you'll do

Maintain deep therapeutic-area expertise by staying current on pre-clinical and clinical data, treatment options, emerging standards of care, and competitive landscape for epilepsy and rare syndromes.
Develop and manage trusted, peer-to-peer relationships with key stakeholders (e.g., KOLs, clinical investigators, medical groups/IDNs, regional payers, patient advocacy groups) and execute tailored engagement plans to identify local needs and opportunities.
Deliver balanced scientific exchange and clinical value propositions, including addressing medical information inquiries and providing effective, audience-tailored presentations to internal and external audiences.
Generate and communicate meaningful medical insights from the field to inform medical strategy and tactics, including input for creation and updates of Standard Response Letters.
Represent UCB as a scientific expert at local, regional, and national conferences and scientific forums, including advisory boards, clinical investigator meetings, roundtables, and educational programs focused on unmet clinical needs.
Identify and support research and educational collaboration opportunities, including feasibility assessment and primary liaison support for unsolicited Investigator-Initiated Studies (IIS) from inception through publication.
Collaborate cross-functionally (e.g., Medical, RWE, access, and other partners) to enhance patient care, support access engagements with medical expertise as needed, and contribute to broader Medical Affairs projects.

Who you'll work with
Internal partners: Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g., sales, marketing, market access).
External partners: healthcare providers and key opinion leaders (KOLs), clinical investigators, medical decision-makers in health systems/IDNs, and patient advocacy organizations.


Interested? For this role, we're looking for the following education, experience, and skills
Minimum Qualifications
Doctorate degree (PhD, PharmD, MD, DPM, or DO).
2 years of medical affairs experience in biopharmaceutical industry.
Must reside within the assigned territory.
Valid driver's license and ability to travel 60-80% in the designated territory.

Preferred Qualifications
Relevant therapeutic area experience.
Prior product launch experience.
Strong business acumen with a solid understanding of the pharmaceutical industry.
Basic knowledge and understanding of health economic principles and clinical trials.
Ability to clearly articulate complex scientific concepts in 1:1 and group settings.
Strong interpersonal skills and excellent verbal and written communication skills.
Creative approach to problem solving and able to work effectively in a constantly changing environment.
Must be a strong team player and effectively interface with other internal departments including regional business units, marketing, sales, medical affairs, and clinical operations.
Strong time management and organizational skills with proficiency in Microsoft applications.
Must complete initial training and successfully pass all assessments within 90 days of hire.

This position's reasonably anticipated salary range is $134k-$204k per year. The actual salary offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer.All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.


Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Employment Type: OTHER