Remote Pharmaceutical Clinical Research Associate

Placements24; Lorenziberg; Ibrido; EUR 60.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive salary

Fully remote position

Health, dental, and vision insurance

Mileage and expense reimbursement

Professional growth opportunities

Descrizione del lavoro

Placements24 seeks an experienced Remote Pharmaceutical Clinical Research Associate (CRA) to monitor trial sites, ensure GCP compliance, and support data quality from a fully remote setting. This role emphasizes ethical research and patient safety while enabling flexible remote work from Austria.

Candidates should have at least 3 years of CRA experience, a science/healthcare degree, and thorough knowledge of ICH-GCP guidelines.

Competenze

• Bachelor's degree in a scientific or healthcare-related field is required.
• Minimum of 3 years of CRA experience in the pharmaceutical industry.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Experience with remote monitoring techniques and technologies.
• Excellent communication, interpersonal, and organizational skills.

Mansioni

• Conduct remote site selection, initiation, monitoring, and close-out visits per protocols.
• Ensure data quality, integrity, and accuracy at investigational sites.
• Verify trials are conducted and reported per protocol, SOPs, GCP, and regulations.
• Train site staff on procedures and regulatory compliance.
• Act as primary contact between study team and sites.
• Prepare and submit monitoring reports, review regulatory documents, manage site issues.

Conoscenze

Communication

Time management

Organizational skills

Independent work

Formazione

Bachelor's degree in science/healthcare

Descrizione del lavoro

About the Role

Our client is seeking an experienced Remote Pharmaceutical Clinical Research Associate (CRA) to play a vital role in the execution of clinical trials. In this fully remote position, you will be responsible for monitoring clinical trial sites, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your work will be instrumental in gathering high-quality data that supports the development of new pharmaceutical therapies. This is an excellent opportunity for a motivated CRA who prefers to work remotely and has a strong commitment to ethical research and patient safety.

Key Responsibilities

• Conduct remote site selection, initiation, monitoring, and close-out visits according to clinical trial protocols and SOPs.
• Ensure the quality, integrity, and accuracy of clinical trial data collected at investigational sites.
• Verify that clinical trials are conducted, recorded, and reported in accordance with the protocol, SOPs, GCP, and applicable regulatory requirements.
• Train and provide guidance to site staff on study-related procedures and regulatory compliance.
• Act as the primary point of contact between the study team and the clinical trial sites.
• Prepare and submit monitoring reports, review site regulatory documents, and manage site issues effectively.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 3 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical industry.
• Thorough knowledge of ICH-GCP guidelines and applicable regulatory requirements.
• Experience with remote monitoring techniques and technologies.
• Excellent communication, interpersonal, and organizational skills.
• Ability to travel to sites as needed (though the role is primarily remote).
• Demonstrated ability to work independently and manage time effectively in a remote setting.

Benefits

• Competitive salary and remote work allowance.
• Fully remote position with flexible working hours.
• Comprehensive health, dental, and vision insurance.
• Mileage and expense reimbursement for necessary travel.
• Opportunities for professional growth and development in clinical research.