Pharmacovigilance Clinician
Hippocratic AISalary not specified
Full Time
Expert & Leadership (9+ years)
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Life Sciences, Healthcare, Clinical ResearchIndustries
Requirements
- Bachelor’s degree in Life sciences or a related field (mandatory)
- Fluency in English and German (mandatory)
- Fluency in Spanish (mandatory, as trilingual role requiring English, Spanish, and German)
- Up to 3 years of previous clinical experience
- 1 year of pharmacovigilance experience (highly valued, not mandatory)
Responsibilities
- Process safety data according to applicable regulations, guidelines, SOPs, and project requirements
- Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities
- Ensure compliance with quality, productivity, and delivery standards per project requirements
- Liaise with different functional team members and healthcare professionals to address project-related issues
- Review, assess, and process safety data and information across service lines, received from various sources
- Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members
Skills
Key technologies and capabilities for this role
Questions & Answers
Common questions about this position
Is this a remote position?
Yes, this is a 100% remote role with work flexibility.
What are the language requirements for this role?
Fluency in English and German is mandatory, and this is a trilingual role requiring fluency in English, Spanish, and German.
What qualifications are needed for this position?
A Bachelor’s degree in Life sciences or a related field is mandatory, along with up to 3 years of previous clinical experience; 1 year of pharmacovigilance experience is highly valued but not mandatory.
What benefits does IQVIA offer for this role?
Benefits include OSDE 310, annual bonus by performance, salary adjustments during the year according to inflation rates, and 21 vacation days.
What experience makes a strong candidate for this Pharmacovigilance Specialist role?
Candidates with a Bachelor’s in Life Sciences, fluency in English and German (plus Spanish), up to 3 years of clinical experience, and especially 1 year of pharmacovigilance experience will stand out.
IQVIA
Advanced analytics and clinical research services
About IQVIA
IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.
Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees