Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

German-Speaking-Pharmacovigilance-Team-Lead-Budapest

Cognizant
Cognizant
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.