Clinical Trial Hub Safety Associate

Pfizer is seeking a highly motivated and detail-oriented individual to join our team as a Clinical Trial Hub Safety Associate. This role is vital to ensuring the safety and well-being of patients participating in our clinical trials. We are looking for a candidate who is passionate about making a difference in the healthcare industry and has a strong understanding of clinical trial safety regulations. If you are someone who thrives in a fast-paced, collaborative environment and has a strong attention to detail, we encourage you to apply for this exciting opportunity.

1. Monitor and track safety data for patients participating in clinical trials, ensuring timely and accurate reporting to regulatory agencies and internal stakeholders.
2. Conduct thorough and timely review of safety data, including adverse events, laboratory results, and concomitant medications, to identify potential safety concerns.
3. Collaborate with cross-functional teams, including clinical research associates, medical monitors, and data managers, to ensure the safety of patients enrolled in clinical trials.
4. Serve as the primary point of contact for safety-related inquiries from internal and external stakeholders, providing prompt and accurate responses.
5. Ensure compliance with all relevant safety regulations, guidelines, and company policies.
6. Assist in the development and review of safety protocols and procedures, as well as contribute to the creation of safety training materials for clinical trial staff.
7. Participate in safety review meetings and provide input and recommendations for risk management and mitigation strategies.
8. Maintain accurate and up-to-date documentation of safety data and activities, including adverse event reports and safety assessments.
9. Continuously monitor safety trends and identify potential areas for improvement, providing recommendations to enhance the safety monitoring process.
10. Act as a safety subject matter expert and provide guidance and support to team members and colleagues as needed.
11. Remain current on industry developments and changes in safety regulations, and proactively communicate any updates or changes to relevant stakeholders.
12. Contribute to the overall success of the clinical trial team by taking on additional responsibilities and tasks as needed.

According to JobzMall, the average salary range for a Clinical Trial Hub Safety Associate in San José Province, Escazu, Costa Rica is between $2,000 to $3,500 per month. This can vary depending on the individual's level of experience, education, and specific job duties. Some Clinical Trial Hub Safety Associates may also receive additional benefits such as health insurance and bonuses.

Pfizer Inc. is an American multinational pharmaceutical corporation headquartered in New York City, with its research headquarters in Groton, Connecticut. It is one of the world's largest pharmaceutical companies.