Clinical Research Associate (Freelance Role) at Biomapas

, , Azerbaijan -

Full Time

Start Date

Immediate

Expiry Date

22 Dec, 25

Salary

0.0

Posted On

23 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Regulatory Compliance, Monitoring, Data Integrity, Patient Safety, Good Clinical Practice, Organizational Skills, Time Management, Teamwork, Electronic Data Capture Systems, MS Office, Communication, Clinical Trial Submission, Site Initiation, Close-Out Visits, Study Documentation

Industry

Research Services

Description

Freelance opportunity in Azerbaijan! Interested to join our Clinical Operations team as a Clinical Research Associate (CRA) with regulatory and start up experience in Azerbaijan? Clinical Research Associate is responsible for monitoring clinical trials and ensuring compliance with regulatory requirements, study protocols, and standard operating procedures (SOPs). This is a position for the potential activities in Azerbaijan, working in close collaboration Clinical Operations team. You have energy and motivation to work in a team and to gain more experience? Submit your CV in the English language for consideration. Responsibilities: · Consulting of Clinical Operations team in country regulatory and start up requirements. · Prepare clinical trial submission dossier and conduct CA and EC submission. · Monitor clinical trials in accordance with regulatory and company guidelines. · Conduct site initiation, monitoring, and close-out visits. · Evaluate and ensure compliance with the study protocols, data integrity, and patient safety. · Maintain communication with clinical trial sites and address any issues that arise. · Collect, review, and verify clinical data for accuracy and completeness. · Assist in the preparation of study documentation and reports. · Keep updated with industry guidelines and regulatory changes. · University degree in Life Sciences, Nursing, or related field. · Fluent written and spoken English and native Azerbaijani. · At least 1-2 years of experience as a Clinical Research Associate or in a similar role. · Strong understanding of Good Clinical Practice (GCP) and regulatory requirements. · Excellent organizational and time management skills. · Ability to work independently and as a part of a team. · Proficient in using electronic data capture systems and MS Office.

Responsibilities

The Clinical Research Associate is responsible for monitoring clinical trials and ensuring compliance with regulatory requirements, study protocols, and standard operating procedures. This includes consulting the Clinical Operations team, preparing submission dossiers, conducting site visits, and maintaining communication with trial sites.