Employer Industry: Clinical Research and Pharmaceutical Development

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Supportive and collaborative work environment
- Chance to make a positive impact on patient safety and health outcomes
- Involvement in meaningful work that contributes to global health and safety
- Comprehensive training programs provided, including GCP and role-specific training

What to Expect (Job Responsibilities):
- Support timely and accurate Drug Safety reporting for adverse events, ensuring adherence to safety reporting plans
- Demonstrate proficiency with standard tools and software systems used for Drug Safety functions and reporting
- Provide data entry and questionnaire transfer support for incoming Targeted Adverse Events
- Assist in the creation of electronic backup files and adjudication packets for reported adverse events
- Participate in departmental strategic planning, problem-solving, and quality improvement initiatives

What is Required (Qualifications):
- Bachelor’s Degree (or relevant alternate concentration)
- Entry-level experience in a related field
- Completion of GCP, MedDRA, and other role-specific training programs as assigned
- Highly organized and detail-oriented with excellent time management skills
- Strong written and verbal communication skills

How to Stand Out (Preferred Qualifications):
- Proficiency in MS Office: Word, PowerPoint, Excel, Access, and MS Project
- Ability to work independently as well as part of a team

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