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Research Scientist

Job Description

We’re seeking a CRP/CRS to temporarily join our Medical Dermatology team in the UK. In the current environment we will open up for candidates from a broader geography by proposing a hybrid model comprising working from home and travel into the office as needed/when the external environment allows.
In this role the CRP/CRS will work as a part of a UK Medical Dermatology team to support Talts PsO and Olumiant AD together with the broader UK Dermatology team. Experience in dermatology is therefore needed. We’re seeking a candidate with engagement for and interest in working as part of a Medical Dermatology team with the aim of converging two dermatology brands into one Dermatology to best serve our customers and patients. The CRP/CRS will report to the Medical Lead Immunology of the UK hub.

Qualifications:
• An advanced medical/scientific or related graduate degree such as MD, PhD, PharmD, Masters degree (degree related to Immunology preferred)

• CRP, CRS, Medical Advisor experience, preferentially in dermatology with knowledge of Taltz PsO and Olumiant AD clinical data. Other candidates with relevant experience might be considered based on profile and experience
• Demonstrated ability to balance scientific priorities with business priorities
• Strong understanding of medical’s role in the cross functional team, and willingness to contribute to the cross-functional work needed to best support our dermatology brands
• Demonstrated strong communication, interpersonal, teamwork, organizational and negotiation skills
• Demonstrated ability to influence others
• Ability to engage in domestic and international travel to the degree appropriate to support the business of the team.
• Fluent in English, verbal and written communication.

Responsibilities:
The primary responsibility is to provide expert medical expertise to all aspects of the local business, to ultimately enhance the customers’ experience in interacting with the company.This includes local marketed product focus, medical support for regulatory affairs and interactions with government agencies, medical expertise for pricing, reimbursement and access (PRA) and leading local scientific data dissemination.
Business/ customer support (pre and post launch support)
• Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, health care providers)
• Actively address customer questions in a timely fashion by leading data analyses and new clinical or health outcomes research efforts.
• Contribute to the development of medical strategies to support brand commercialization activities
• Support training of sales representatives, and other medical representatives.
• Contribute as a scientific and medical expert to activities and deliverables of the PRA organization, in particular giving clinical input and insight to develop payer partnership programs and defend the product value.
• Contribute actively on an ongoing basis to the strategic planning for currently marketed brands.
• Offer scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team.

Scientific Data Dissemination/Exchange
• Knowledge of compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals. Review and approve promotional and non-promotional materials in line with the local compliance guidelines.
• Support the planning of symposia, advisory board and medical meetings
• Support medical information associates in preparation and review of medical letters and other medical information materials.
• Support training of local medical personnel
• Prepare or review scientific information in response to customer questions or media requests
• Support data analysis and the development of slide sets
• Develop and maintain appropriate collaborations and relationships with relevant professional societies.

Clinical Planning
• Communicate and collaborate to ensure life cycle plans for drugs in development address customer needs
• Collaborate with other regions and the global teams

Clinical Research/Trial Execution and Support
• Review and approve local informed consent documents
• Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials

Regulatory Support Activities
• Participate in development and review of local labeling and labeling modifications
• Provide medical expertise to regulatory scientists.
• Support / assist in the preparation of regulatory reports

Scientific / Technical Expertise and continued development
• Be aware of current trends and projections for clinical practice
• Keep updated with medical and other scientific developments relevant to the product.

Employment Type: Contract Based
Contact Information
Name: PE Global team