Medical and Scientific Reviewer

**Company Description**
At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than 7,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We are grounded in our cultural beliefs and serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills and talents are unique, but together we make an impact every day. Join us

Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs. We are deliberate and self-reflective about the kind of team and culture we are building. We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve. We are EVERSANA.

THE POSITION:
At EVERSANA, we provide end-to-end integrated global medical information and medical affairs services
for various life sciences companies, including pharmaceutical, biotechnology, medical device, digital
therapeutics, and over-the-counter companies of various sizes, including industry leaders and emerging
companies. Additionally, we provided therapeutic area support across oncology, hematology, rare
diseases, immunology, cardiology, dermatology, urology, gastroenterology, infectious diseases,
nephrology, neurology, pain, rheumatology, respiratory, ophthalmology, endocrinology, pulmonology,
hepatology, consumer products, woman’s health and more.
This position will be part of our global medical content development and medical / scientific review team.
This role requires medical and scientific expertise, an understanding of regulations and best practices for
promotional and non-promotional materials, high attention to detail and medical / scientific accuracy, the
ability to analyze / translate / interpret scientific literature and data, the ability to quickly learn new
therapeutic areas, and excellent communication skills (both verbal and written).

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Our employees are tasked with delivering excellent business results through the efforts of their teams.
These results are achieved by:
Perform scientific data fact-checking and review of promotional and non-promotional
materials that are submitted for medical, legal, and regulatory (MLR) review meetings.
Ensure that data are scientifically accurate, contextually correct, editorially accurate, and are
presented in a fair/scientifically balanced manner with mínimal supervision and in a timely
manner:

- Ensures scientific accuracy, relevance, and completeness of data
- Ensures claims and data are clinically and statistically relevant and presented in a
scientifically balanced manner (not false or misleading)
- Ensures that claims are adequately supported by data
- Determines acceptability of references
- Advises on whether claims are consistent with the approved label
- Ensure that the piece is relevant and of utility for the target audience
Ensure that information and data presented aligns and are consistent with the client’s
medical strategy for the review of promotional and non-promotional materials across different
therapeutic areas and brands to ensure that materials are of high quality and in compliance
with applicable laws and regulations, industry standards, and best practices.
Review materials, proofread, and check medical content/claims against references.
Collaborate and partner with internal or client medical signatory reviewers to ensure
alignment and timely and efficient turnaround of material review.
Collaborate with material owners / sponsors and other MLR team members to resolve
findings, in collaboration with the medical signatory reviewer.
Identify, communicate, and resolve issues impacting timelines.
Propose recommendations for content and process improvements that could reduce
recurring errors and issues.
Work with EVERSANA and/or client-provided document management technology platforms
(i.e., Veeva PromoMats / MedComms) as content owner when appropriate, uploading
documents, and providing reference anchoring and annotations as required.
Collaborate with the Head of Medical Content Development / Medical Affairs / Medical
Information and contributes to discussions on strategy, tactical execution and communication
approaches for assigned projects.
Participate in key client meetings as assigned.
Support content creation for Medica