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

📋 Description

• Coordinates, supervises, and completes tasks related to assigned trials.

• Conducts file reviews and documents outcomes.

• Ensures that assigned tasks are completed on schedule and within budget.

• Provides system support and ensures that system databases are up to date.

• Analyzes and reconciles study metrics and assists with issues related to site documentation.

• Maintains awareness of SOPs and current regulatory requirements.

• Assists the start-up team with regulatory submissions.

• Collaborates directly with sites to gather necessary documentation.

• Records communication and follows up with site contacts.

• Trains new staff on processes and systems.

⛳️ Requirements

• High school diploma or equivalent, along with relevant formal academic or vocational qualifications.

• Bachelor's degree is preferred.

• Previous experience (0 to 1 year) or equivalent experience is considered adequate.

• Strong organizational skills and keen attention to detail.

• Ability to work collaboratively in a team or independently.

• Proven ability to effectively analyze project-specific data and systems.

• Must have a strong customer focus and proficient English language skills.

• Proficient in MS Office applications (Word, Excel, and PowerPoint).

• Must successfully complete the organization's clinical training program.

🏝️ Benefits

• Health insurance

• Retirement plans

• Paid time off

• Flexible work arrangements

• Professional development