Job Description
A scientific/strategic contributor with broad expertise and/or unique knowledge in a specific area, and an ability to achieve objectives in creative and effective ways. Typically manages multiple projects within a client or within a specialized area across several clients. Acts as the client’s primary point of contact for engagements, developing mutually beneficial partnerships and taking ownership for the needs of the client.
Responsibilities
Job Responsibilities
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Responsible for independently (most of the time) leading projects (up to 5-6 mid-size projects) involving literature reviews, including systematic literature reviews (SLRs) on various topics and indications
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As project lead, responsible for client communication, overall project management and operations, coordination of project day-to-day activities, and quality of deliverables
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Provide senior-level quality review and methodological guidance to junior team members, supporting technical capability development and ensuring consistent scientific rigor across project deliverables
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Responsible for conducting and leading HTA-compliant and EU-JCA compliant SLR packages
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Master 80% of the techniques used in his/her specialty
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Collaborates closely with other senior members to determine to support business development activities, such as proposal development, project scoping, capabilities/demo presentations
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Responsible for line management and mentoring of 1-2 junior research consultants or research associates
Qualifications
Qualifications
Education: Master’s degree in Pharmacology, Biochemistry, Epidemiology, Health Economics or other relevant scientific field. PhD or MD highly desirable.
Experience: 4-5 years of experience at a minimum in the clinical trials or health research or consulting environment. May require additional experience depending on focus area.
Skills
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Thorough understanding of the biopharmaceutical R&D process combined with business acumen.
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Comfortable presenting and interfacing with senior executives within the clients. Strong technical writing, oral communication and presentation skills, excellent use of the English language.
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Interest and familiarity with AI and its use to support literature review, including published guidelines.
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Curious, collaborative, entrepreneurial and self-motivated, without the need for significant infrastructure and support, and with an understanding of the dynamics of high-growth companies; the ability to work effectively in a demanding, challenging, rapidly changing environment.
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Strong interpersonal skills with the ability to gain respect of personnel at all levels and collaborate efficiently within a large team.
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Strong problem-solving and analytical skills, and the ability to execute in complex situations
Senior Research Consultant, Evidence Review and Software employer: Cytel
Cytel is an exceptional employer that empowers its employees to thrive in a collaborative and innovative environment, particularly for the role of Principal SAS Programmer. With a strong commitment to professional development and training, Cytel ensures that you have the support needed to excel in your career while working remotely with a leading global pharmaceutical client. The company values diversity of thought and encourages autonomy, making it an ideal place for those looking to make a meaningful impact in the field of clinical trials.
