Senior Research Consultant, Evidence Review (REMOTE Canada only)
About the role
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
- 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
- As project lead, responsible for client communication, overall project management and operations, coordination of project day-to-day activities, and quality of deliverables
- Responsible for conducting and leading HTA-compliant and EU-JCA compliant SLR packages
- Master 80% of the techniques used in his/her specialty
- Collaborates closely with other senior members to support business development activities, such as proposal development, project scoping, capabilities/demo presentations
- Responsible for line management and mentoring of 1-2 junior research consultants or research associates
Qualifications
- Master’s degree in Pharmacology, Biochemistry, Epidemiology, Health Economics or other relevant scientific fields.
- PhD or MD is highly desirable.
- 4-5 years of experience at a minimum in the clinical trials or health research or consulting environment. May require additional experience depending on the focus area.
- Thorough understanding of the biopharmaceutical R&D process combined with business acumen.
- Comfortable presenting and interfacing with senior executives among the clients. Strong technical writing, oral communication and presentation skills, excellent use of the English language.
- 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.
- Strong interpersonal skills with the ability to gain respect for personnel at all levels and collaborate efficiently within a large team.
- Strong problem-solving and analytical skills, and the ability to execute in complex situations.
About Cytel
Cytel is the world’s leading data-science CRO, driving advancements in human health through robust analytics and innovative clinical trial software. For nearly four decades, we have set the standard in adaptive trial design, leveraging extensive data insights to inform strategy throughout every phase of drug development and commercialization. Our mission is clear: accelerate drug development, enhance success rates, and deliver better patient outcomes. With a comprehensive suite of services from innovative trial design to end-to-end biometrics and real-world evidence, our specialized, multidisciplinary team ensures optimal strategies for preclinical research, trial execution, market access, and reimbursement.
Headquartered in Cambridge, Massachusetts, Cytel has a global presence with over 2,000 employees across North America, Europe, and Asia. Learn more about how Cytel is harnessing the power of data to advance human health at www.cytel.com.
Senior Research Consultant, Evidence Review (REMOTE Canada only)
About the role
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
- 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
- As project lead, responsible for client communication, overall project management and operations, coordination of project day-to-day activities, and quality of deliverables
- Responsible for conducting and leading HTA-compliant and EU-JCA compliant SLR packages
- Master 80% of the techniques used in his/her specialty
- Collaborates closely with other senior members to support business development activities, such as proposal development, project scoping, capabilities/demo presentations
- Responsible for line management and mentoring of 1-2 junior research consultants or research associates
Qualifications
- Master’s degree in Pharmacology, Biochemistry, Epidemiology, Health Economics or other relevant scientific fields.
- PhD or MD is highly desirable.
- 4-5 years of experience at a minimum in the clinical trials or health research or consulting environment. May require additional experience depending on the focus area.
- Thorough understanding of the biopharmaceutical R&D process combined with business acumen.
- Comfortable presenting and interfacing with senior executives among the clients. Strong technical writing, oral communication and presentation skills, excellent use of the English language.
- 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.
- Strong interpersonal skills with the ability to gain respect for personnel at all levels and collaborate efficiently within a large team.
- Strong problem-solving and analytical skills, and the ability to execute in complex situations.
About Cytel
Cytel is the world’s leading data-science CRO, driving advancements in human health through robust analytics and innovative clinical trial software. For nearly four decades, we have set the standard in adaptive trial design, leveraging extensive data insights to inform strategy throughout every phase of drug development and commercialization. Our mission is clear: accelerate drug development, enhance success rates, and deliver better patient outcomes. With a comprehensive suite of services from innovative trial design to end-to-end biometrics and real-world evidence, our specialized, multidisciplinary team ensures optimal strategies for preclinical research, trial execution, market access, and reimbursement.
Headquartered in Cambridge, Massachusetts, Cytel has a global presence with over 2,000 employees across North America, Europe, and Asia. Learn more about how Cytel is harnessing the power of data to advance human health at www.cytel.com.