Research Assistant

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

📋 Description

• Identify, recruit, educate, and pre-screen candidates for participation in a study.

• Analyze, comprehend, and be well-versed in the study protocol and related diseases to effectively inform patients and their families.

• Record all patient interactions accurately and in compliance with GCP and ALCOA-C standards.

• Keep information current across various study platforms.

• Participate in regularly scheduled meetings with Principal Investigators and their site teams.

• Negotiate contracts with prospective facilities.

• Assist in the preparation of regulatory documents and secure signatures from necessary personnel.

⛳️ Requirements

• At least 2 years of relevant experience in clinical research.

• Highly skilled in utilizing various technologies for clinical research, including recruitment platforms, IWRS, EDC, and other clinical trial software.

• Proficient in Microsoft Office applications (Word, Outlook, Teams, and Excel).

• Strong customer service and communication skills.

• Knowledgeable in research terminology and basic medical language.

• Understanding of the overall clinical development framework and a solid grasp of government regulations, GCP, and ALCOA-C.

• Excellent organizational and time management abilities.

• High attention to detail.

• Capable critical thinker and problem solver.

• Proper home office setup, including a private area for participant communication and high-speed internet (minimum: 100MB up and 15MB down, 5 GHz router).

• Fluency in Spanish is an added advantage.

🏝️ Benefits

• Paid Time Off (PTO) and Company Paid Holidays.

• 100% Employer-paid medical, dental, and vision insurance plan options.

• Health Savings Account and Flexible Spending Accounts.

• Bi-weekly employer contributions to HSA.

• Company-covered Short-Term and Long-Term Disability.

• 401(k) Retirement Plan with Company Match.