Research Manager-Real World Evidence
at Lumanity
London SE1, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 26 Nov, 2024 | Not Specified | 31 Aug, 2024 | N/A | Research Projects,Compliance Procedures,Writing,Publications | No | No |
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Description:
Overview / About us:
Lumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies around the world to generate evidence to demonstrate the value of their product, translate the science and data into compelling product narratives, and enable commercial decisions that position these products for success in the market. We do this through strategic and complimentary areas of focus: Strategic Consulting & Insight, Value, Access, & Outcomes, Medical Strategy & Communications, and Real-World Evidence.
The PHARMO Institute, part of Lumanity, uses data to derive real-life insights into value of medicines. We provide tailor-made research solutions for: post-authorization safety and efficacy (PASS, PAES) and drug utilization review (DUR); incidence/prevalence, treatment patterns, and patient pathways; comparative effectiveness, including synthetic control arms; healthcare resource use and cost of illness research; validation of surrogacy outcomes; as well as AI patient finding, classification, and disease progression prediction. PHARMO is a one-stop shop to coordinate your global observational research needs by leveraging its extensive data partner network and academic links to clinician/KOL experts. PHARMO provides medical writing, scientific publications, and literature review services, as well as a host of strategic commercialization services with Lumanity.
Responsibilities / Position overview:
We are seeking a Research Manager to conduct and supervise pharmacoepidemiolgic research for our clients using various proprietary databases. In this role, you are responsible for complex partial or final reports within larger projects, including the quality of the substantive result and the implementation process. This role includes some project management responsibilities, and will lead other employees involved in the research process on less complex or parts of complex projects.
You will also be expected to contribute to the innovations within the business, contribute to workshops, and write publications.
Qualifications:
- Completed academic training in the field of medical content
- Masters the Dutch and English language (word and writing)
- Knowledge and experience with epidemiological/RWE/statistical research, preferably registered Epidemiologist (level A)
- Experience with the execution of research projects
- Experience in writing publications and giving lectures
- Adheres to security and compliance procedures
Benefits:
We offer our employees a comprehensive benefits package that focuses on what matters to you – health and well-being, personal finances, professional development, and a healthy work/life balance:
- Competitive salary
- Attractive pension scheme
- Positive working atmosphere with committed colleagues and an enthusiastic management team.
- Flexible working hours and the possibility to work partly from home
- a role in which you can combine your programming knowledge, passion for data, commercial craftsmanship and social involvement
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
London SE1, United Kingdom