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Clinical Development Center Project Manager

3-5 years
Not Disclosed
10 July 8, 2025
Job Description
Job Type: Full Time 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

 

Clinical Development Center Project Manager – Seoul (1.5-Year Contract)

Job Summary:
Novo Nordisk is seeking a detail-oriented and motivated Clinical Development Center (CDC) Project Manager to oversee clinical trials in South Korea. This 1.5-year contract-based role is ideal for professionals experienced in clinical operations, regulatory compliance, and trial execution. You’ll play a pivotal role in ensuring the successful planning, execution, and delivery of multiple trials in accordance with ICH-GCP standards and Novo Nordisk SOPs.


Key Responsibilities:

  • Oversee end-to-end management of assigned clinical trials, from site selection to trial close-out

  • Ensure regulatory compliance, timeline adherence, and budget tracking for assigned studies

  • Serve as the main liaison with CRAs, HQ Trial Managers, and Therapeutic Area Managers

  • Coordinate feasibility assessments, resource planning, and risk assessments

  • Monitor subject recruitment, retention, and data quality to meet study milestones

  • Manage local CRO/vendor relationships and ensure timely CTMS, EDC, and eTMF updates

  • Handle regulatory document submissions and approvals in alignment with GCP standards

  • Provide consolidated country input during trial design and execution phases

  • Escalate and resolve operational issues with local/HQ stakeholders

  • Track and report progress, ensuring cost-effectiveness and operational excellence


Required Skills & Qualifications:

  • Bachelor’s degree in Pharmacy, Life Sciences, Nursing, or related field

  • Solid experience in clinical trial monitoring and trial management in line with ICH-GCP

  • Proven knowledge of trial methodology, regulatory processes, SOPs, and clinical operations

  • GCP-certified with strong understanding of the drug development lifecycle

  • Proficiency in clinical systems: SAP, CTMS, EDC, eTMF

  • Strong communication skills in English, both written and verbal

  • Ability to work independently and proactively drive results under pressure


Perks & Benefits:

  • Work with a globally renowned pharmaceutical leader

  • Exposure to international clinical development programs

  • Collaborative and diverse work culture

  • Learning and development opportunities

  • Competitive contract-based compensation


Company Overview:

Novo Nordisk is a global healthcare leader with over 100 years of innovation in diabetes care, and a growing focus on obesity, rare blood and endocrine disorders. Operating in over 170 countries, Novo Nordisk is committed to improving patient lives through science-driven, patient-centric solutions in chronic disease care.


Work Mode: On-site (Seoul, South Korea)
Contract Duration: 1 year 6 months
Preferred Salary/Compensation: Not explicitly mentioned in the description.


Call to Action:

Ready to take on a meaningful role in clinical trial leadership? Apply now to become a part of Novo Nordisk’s mission to change lives through healthcare innovation. Submit your CV through the Novo Nordisk career portal today.