Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Competitive salary and benefits package
- Opportunity for career advancement and growth within the organization
- Various annual leave entitlements to support work-life balance
- Access to a global Employee Assistance Programme for personal and family well-being
- Flexible benefits tailored to individual needs, including health insurance and retirement planning
- Commitment to diversity, inclusion, and a supportive work environment

What to Expect (Job Responsibilities):
- Ensure compliance with ICH/GCP guidelines and applicable regulations for clinical studies
- Contribute to the development and delivery of clinical development strategy
- Build relationships and collaborate with oncology staff across global functions
- Develop and write study protocols, procedures manuals, and clinical study reports
- Act as a subject matter expert to support internal and external customers

What is Required (Qualifications):
- Bachelor’s degree in life sciences or related discipline
- 3-5 years of experience in the pharmaceutical industry or CRO environment
- In-depth knowledge of study management and global regulatory guidelines
- Proven track record of collaboration with investigators and external experts
- Excellent leadership skills

How to Stand Out (Preferred Qualifications):
- Advanced degree (e.g., MS, PhD, PharmD)
- Clinical development experience across all phases of development (I-IV)
- Highly developed communication skills for effective decision-making
- Proven expertise in identifying and addressing clinical program issues
- Excellent influencing and negotiation skills

#ClinicalResearch #Oncology #CareerGrowth #DiversityAndInclusion #WorkLifeBalance

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