Clinical Research - Trials (GCP EDC Trained)

Angel City VA; Philippines; On-site; PHP 481,867 - 686,296; Part time

Benefits offered by this job

Competitive salary and benefits package

Remote work

Professional development opportunities

Supportive work environment

Job summary

Angel City VA is looking for a Medical Virtual Assistant with expertise in GCP or EDC to manage clinical trials remotely. Responsibilities include coordinating trials, ensuring compliance with guidelines, and maintaining documentation. Applicants should have experience in clinical trials, strong organizational skills, and proficiency with trial management software. Preferred qualifications include a Bachelor's degree in a related field and certification in GCP or EDC. Join us in advancing medical research and improving patient outcomes.

Qualifications

• Proven experience as a Medical Virtual Assistant or similar role in clinical trials.
• In-depth knowledge of GCP guidelines and EDC systems.
• Excellent organizational and time management skills.

Responsibilities

• Assist with the management and coordination of clinical trials.
• Ensure compliance with GCP guidelines and EDC standards.
• Maintain and organize clinical trial documentation.

Skills

Clinical trial management

GCP guidelines

EDC systems

Data entry

Communication skills

Education

Bachelor's degree in life sciences, nursing, or health administration

Certification in GCP or EDC

Tools

Clinical trial management software

Job description

Clinical Research - Trials (GCP EDC Trained)

Medical Virtual Assistant (GCP or EDC) - Must Know Clinical Trials

Are you passionate about clinical trials and eager to make a difference in the medical field? We are looking for a dedicated and skilled Medical Virtual Assistant with expertise in Good Clinical Practice (GCP) or Electronic Data Capture (EDC) to join our dynamic team.

Position: Medical Virtual Assistant (GCP or EDC)

Location: Remote

PayRate: $7 per hour.

Key Responsibilities

• Assist with the management and coordination of clinical trials.
• Ensure compliance with GCP guidelines and EDC standards.
• Maintain and organize clinical trial documentation.
• Communicate effectively with trial sites, sponsors, and other stakeholders.
• Perform data entry, data cleaning, and database management tasks.
• Support the development and review of study protocols, informed consent forms, and other trial-related documents.
• Assist in the preparation of trial progress reports and other regulatory submissions.

Requirements

• Proven experience as a Medical Virtual Assistant or similar role in clinical trials.
• In-depth knowledge of GCP guidelines and EDC systems.
• Familiarity with clinical trial protocols and regulatory requirements.
• Excellent organizational and time management skills.
• Strong attention to detail and accuracy.
• Proficient in using clinical trial management software and tools.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.

Preferred Qualifications

• Bachelor’s degree in a related field (e.g., life sciences, nursing, health administration).
• Certification in GCP or EDC.
• Experience with specific EDC platforms such as Medidata, Oracle Clinical, or REDCap.

What We Offer

• Competitive salary and benefits package.
• Remote work.
• Professional development and growth opportunities.
• A supportive and collaborative work environment.

If you are a proactive and detail-oriented professional with a passion for clinical trials, we encourage you to apply for this exciting opportunity. Join us in our mission to advance medical research and improve patient outcomes.