Description:
Location: Remote, United Kingdom

Schedule: Full-time, Permanent

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it's the best of both worlds….

We have the rare opportunity available within CROMSOURCE for an experienced Real-World Evidence (RWE) Scientist to join us in a sponsor-dedicated capacity with one of our partner pharmaceutical companies.

CROMSOURCE is an international CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts.

Main Job Tasks and Responsibilities:

• Design and execute global real-world evidence projects to inform strategic internal decision-making, thereby empowering differentiating R&D activities, and support external decision making by key stakeholder groups (such as patients, regulators, policy makers, payers, and prescribers)
• Contribute to the wider epidemiological and medical understanding of specific diseases
• Provide input to Global RWE Strategy & Tactical Plan for the respective patient population
• Lead RWE study design, planning and execution, including protocol development and analysis specification following best methodological standards
• Collaborate with RWE contractors and external vendors on RWE projects and providing RWE Analysts with clarifications concerning protocol implementation
• Drive interpretation of analysis in collaboration with RWE Strategy Lead & internal stakeholders, and communicate analysis interpretation internally and externally
• Provide strategic input to internal stakeholders based on RWE activities and robust epidemiological and medical understanding of the patient population in focus
• Represent RWE on functional teams (e.g., Medical Team, Patient Safety, Regulatory, Market Access, Commercial/Marketing, Core Launch Teams, etc.)
• Support RWE Strategy Lead to ensure alignment of RWE tactics with the Strategic Publication Plan
• Drive innovative study designs, including new data sources and advanced analytics (incl. digital pharmacoepidemiology)

Education and Experience:

• You hold a Master degree (ideally a PhD) in Epidemiology, Outcomes Research or other relevant scientific discipline, and have a track record of publications in high-quality peer-reviewed journals
• Experience in having successfully delivered global and/or local RWE projects from conceptualisation to publication within the pharmaceutical industry (or with a recognised expert consultancy or academic centre of excellence), using primary as well as secondary data, such as large healthcare databases
• Hands-on experience in working across internal stakeholder functions (e.g., medical affairs, market access, clinical development, etc.) to develop the optimal RWE strategy and tactical plan to support an asset within a specific disease area or focus
• Combination of strong methodological quantitative knowledge, strategic, innovative thinking, and communication skills
• Background knowledge of industry trends and best practices, specifically related to epidemiology/outcomes research
• Good knowledge and understanding of applicable regulations in pharmacoepidemiology, pharmacovigilance and clinical development
• Expertise in the EU5 and/or US healthcare environment (and changes therein)
• Proven ability to write/edit scientific communications (abstracts, poster presentations, podium presentations, manuscripts, etc.)
• Able to deliver impactful presentations to senior management or industry audiences with a relaxed and proficient presentation style
• Passion for developing and maintaining strong collaborative relationships with key partners and stakeholders based on in-depth understanding of stakeholder needs and strategic focus
• Ability to proactively use his/her relationships with internal and external stakeholder groups to provide strategic input through synthesized thinking, building advocacy and empowering implementation of the solutions in support of creating patient value

Our Benefits:

• Pension contribution
• Life assurance
• 25 days holiday + bank holidays
• Child care vouchers
• Eye-test vouchers
• Seniority bonus
• Excellent work-life balance
• Dedicated Line Manager
• Monthly meetings with line manager
• Full performance and development process with end of year reviews
• Team events and end of year party
• Employee satisfaction survey - your feedback is important for continuous improvement

The Application Process

Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step.

If you would like to discuss the role before applying through the website @ www.cromsource.com/careers/job-vacancies please contact careers@cromsource.com for more information.

Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Key words: Real Word Evidence, Real World Data, Real World Analytics, RWE Expert, RWE Scientist, Epidemiology, Market Access, Health Economics Outcomes Research, HEOR, CER, Secondary Data, Health Insurance Claims, Claims Data, Contract Research Organisation, CRO, Outsourced, Sponsor dedicated, Pharmaceutical, Pharma, Pharmaco
Skills: Scientist, CER, Epidemiology, Pharma, Real World Evidence Location: United Kingdom Share:

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