Office Location: Budapest, Hungary – 9th District, Mill Park Office Building
Working Hours: 40 hours per week
Work Arrangement: 100% Remote
Schedule: Standard business hours
What We Offer
- Competitive salary and cafeteria benefits
- Discounted All You Can Move SportPass
- Comprehensive medical benefits
- Risk and accident insurance coverage
- Opportunity to be part of a rapidly expanding organization
- Continuous training, learning, and certification opportunities
- Multilingual environment with native-speaking colleagues
- Inspiring and pleasant working atmosphere in a multicultural community
- Reimbursable language courses
Essential Qualifications
· Life-Science / Healthcare Professional / Master of Public Health with experience in Literature reviews / Pharmacoepidemiology / Master’s degree in Epidemiology
Preferred Working Experience:
· 2+ years’ experience in performing literature reviews in Epidemiology or Public Health
· Experience in statistical analysis software such as STATA or SAS etc.
Essential skills
· Demonstrates depth and breadth of specialist knowledge of epidemiology and medical statistics
· Demonstrates awareness of the critical appraisal of epidemiological literature and of different study designs commonly used in epidemiological studies
· Fluent English (oral and written)
· Good Understanding of epidemiology
· Experience performing critical commentaries of studies (limitations, implications and conclusions)
· Ability to critically appraise and synthesize epidemiological literature
· Ability to write research reports and to effectively disseminate outcome
· Strong interpersonal and communication skills
· Initiative for process improvement
· Ensure customer satisfaction
· Good team worker
· Good business ethics
· Literature reviews as requested by client epidemiologists using the best practice methodologies
· Literature search and preparation of Literature review report for Pharmacoepidemiology
Responsibilities
· Literature reviews as requested by client epidemiologists using the best practice methodologies
· Literature search and preparation of Literature review report for Pharmacoepidemiology
· Perform peer Scientific & Technical Review
· Follows the processes and requirements as outlined in the client guidance documents on Literature Reviews
· Provides review reports in format and quality as described in the guidance document
· To collaborate with the client epidemiologist(s) to define timelines for the literature reviews, to clarify questions, to provide feedback
· Understanding the disease area and therapeutics compound’s mode of action as applicable
· Attending, along with supervisor if required, Safety Management Team (SMT) meetings as applicable
· Discussing any comments regarding the literature review (including epidemiological interpretation) with the Safety Management Team SMT as applicable
· Working independently / directly / in consultation with Medical Writer, Regulatory Team, Global Pharmacovigilance Safety Lead or Scientific and Operational Epidemiology Lead for epidemiological evidence review projects i.e. drug Safety Profile Plans (dSPP), Risk Management Plans (RMP), Orphan Drug Application (ODA), Pregnancy and Lactation Labeling Rule (PLLR) updates or Pediatric Investigation Plans (PIP)
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What we offer
- The chance to work with impact. Here, you’re empowered to bring your biggest thinking to help our company and clients improve everyday life.
- Ownership over your career. Stay at the top of your game through our award-winning learning and development ecosystem. And when your ambitions change or we offer new opportunities, we help you pivot by providing reskilling, on-the-job learning and guidance to find new roles that might be a better fit.
- The opportunity to thrive on a high caliber team with heart. We celebrate each other’s experiences and perspectives and promote a sense of belonging through our affinity groups and diversity and inclusion initiatives.
- A comprehensive total rewards package, including a competitive salary and a pension plan with matching contributions.
- Flexible health and financial benefits to support you and your eligible dependents—from day one.
- True work-life balance. Be at your best through paid time off, flexible work arrangements, volunteering opportunities, social events, and so much more.
About us
Cognizant (Nasdaq: CTSH) is an AI Builder and technology services provider, building the bridge between AI investment and enterprise value by building full-stack AI solutions for our clients. Our deep industry, process and engineering expertise enables us to build an organization’s unique context into technology systems that amplify human potential, realize tangible returns and keep global enterprises ahead in a fast-changing world. See how at www.cognizant.com or @cognizant.
Other employment-related information
Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, provincial or local laws.
If you have a disability that requires reasonable accommodation to search for a job opening or submit an application, please email [email protected] with your request and contact information.
Language requirements vary depending on roles, but we ask that all candidates have basic English proficiency for company-wide communications purposes. For roles based in Quebec, professional English proficiency is required, as you’ll deliver services to and collaborate with stakeholders outside the province who may not speak French.
