Study Delivery Specialist I

This is a fully remote position, open to applicants in Mexico.

📋 Description

• Assist in overseeing clinical trial sites.

• Ensure compliance with study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

• Support site management tasks, including documentation preparation, data entry, and monitoring site performance metrics.

• Collaborate with cross-functional teams to enhance communication and resolve site-related challenges.

• Maintain precise records of site activities and contribute to monitoring reports.

• Engage in training and development initiatives to improve knowledge and skills in clinical trial management.

⛳️ Requirements

• Bachelor's degree in a relevant discipline such as life sciences, healthcare administration, or clinical research.

• Some experience in clinical research, site management, or similar administrative roles is preferred but not essential.

• Strong organizational abilities and attention to detail, with the capacity to manage multiple tasks effectively.

• Basic understanding of clinical trial processes and regulatory requirements is advantageous.

• Excellent communication and interpersonal skills, with the ability to work collaboratively in a team setting.

• Willingness to travel as necessary (approximately 25%).

• Legal authorization to work in Mexico.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.