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German-Speaking-Pharmacovigilance-Team-Lead-Budapest

2-4 years
Not Disclosed
10 June 27, 2025
Job Description
Job Type: Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Process Specialist – Clinical Data Management / Pharmacovigilance (Hybrid)

Location: Hybrid | Full-Time | Rotational Shifts | No Travel Required

Job Summary:
Cognizant is hiring a Process Specialist in CDM/Pharmacovigilance to strengthen its Pharma Research & Development services. Ideal for professionals with 2–4 years of experience in PV case processing and safety operations, this role demands a deep understanding of pharma regulations, analytical skills, and the agility to work in a hybrid model with rotational shifts. If you're passionate about enhancing drug safety and improving operational efficiency, this role offers the perfect growth platform.


Key Responsibilities:

  • Manage and optimize pharmacovigilance and clinical data management processes in line with compliance standards

  • Support pharmacovigilance case processing with accurate documentation and timely submissions

  • Collaborate with cross-functional teams to streamline workflows and ensure regulatory adherence

  • Analyze safety data, prepare reports, and contribute to strategic planning and decision-making

  • Implement process enhancements and monitor performance to drive continuous improvement

  • Coordinate process communication across departments for seamless operations

  • Maintain and develop SOPs to ensure quality and consistency

  • Support team training and development initiatives for ongoing PV knowledge upgrades

  • Participate in rotational shifts to support global operations across time zones


Required Skills & Qualifications:

  • Bachelor's or advanced degree in Pharmaceutical Sciences, Life Sciences, or related fields

  • 2 to 4 years of experience in the pharmaceutical industry, preferably in pharmacovigilance or safety operations

  • Proficient in PV case processing, safety data documentation, and regulatory requirements

  • Strong analytical mindset and familiarity with pharma compliance standards

  • Excellent communication and teamwork skills

  • Ability to work in rotational shifts and a hybrid model

  • Familiarity with PV tools and industry-standard software

  • Self-starter with a keen eye for process improvement and operational accuracy


Perks & Benefits:

  • Competitive salary and benefit package (including annual bonus)

  • Hybrid work flexibility

  • Free medical benefits and accident insurance

  • Reimbursable language courses and professional development support

  • Training and certification programs

  • Access to All You Can Move SportPass at discounted rates

  • Company-wide recognition, team events, and a positive work culture

  • Opportunity to work in a multilingual, collaborative environment


Company Description:

Cognizant is a global leader in digital healthcare transformation, pharmacovigilance, and pharmaceutical process management, serving top-tier life sciences clients. With a presence in over 35 countries and 300,000+ professionals, Cognizant enables smarter, safer drug development through cutting-edge technology and expert operations.


Work Mode: Hybrid (Rotational Shifts | No Travel)


Call-to-Action:

Accelerate your career with Cognizant and make a direct impact on global pharmacovigilance and clinical data operations. Apply now for the Process Specialist-CDM/PV role and become a key player in shaping drug safety excellence.