Clinical Research Associate Armenia at Biomapas

, , Armenia -

Full Time

Start Date

Immediate

Expiry Date

20 Apr, 26

Salary

0.0

Posted On

20 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Good Clinical Practice, Data Integrity, Patient Safety, Regulatory Compliance, Monitoring Visits, Site Assessments, Training, Mentoring, Communication, Organizational Skills, Time Management, Electronic Data Capture Systems, Microsoft Office Suite, Independent Work, Team Collaboration, Travel

Industry

Research Services

Description

Join our dynamic team at Biomapas as a Clinical Research Associate (CRA) in Armenia. Your role will be crucial in overseeing clinical trials and ensuring that they are conducted in compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Position is open for Armenia. All CV's needs to be submitted in English language. Responsibilities: Conduct site assessments, initiate, monitor, and close-out clinical sites to ensure compliance with clinical protocols and regulatory guidelines Perform regular monitoring visits, ensuring data integrity, patient safety, and adherence to trial protocols Review and verify that clinical trial data is accurate, complete, and entered correctly into the database Act as the main point of contact for clinical trial sites, addressing inquiries, issues, and providing support throughout the study Assist in the training and mentoring of junior CRAs and site staff Prepare and submit reports to management on the progress of clinical trials, including any potential issues Ensure all necessary documentation is maintained and is audit-ready Stay updated with industry trends and regulatory changes impacting clinical research Bachelor’s degree in Life Sciences, Nursing, or related field Minimum 2 years of experience as a Clinical Research Associate (CRA) in a pharmaceutical or clinical research organization Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements Excellent communication, organizational, and time management skills Proficient in electronic data capture systems, and familiarity with Microsoft Office Suite Ability to work independently and within a team environment Willingness to travel to clinical trial sites as needed Professional growth and career opportunities International team and environment Bonus based on annual performance Personal accident and business trip insurance Additional health insurance Remote/home based Complimentary health and wellness benefits, such as influenza vaccines Rewarding referral policy Workplace establishment allowance (fully remote) Team building, global meetings, B active events

Responsibilities

The Clinical Research Associate will oversee clinical trials, ensuring compliance with protocols and regulatory guidelines. Responsibilities include conducting site assessments, monitoring visits, and acting as the main point of contact for clinical trial sites.