Remote Clinical Research Associate - Pharmaceutical Trials

Placements24; Sudáfrica; A distancia; ZAR 420.000 - 720.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Remote work

Medical aid contributions

Performance bonuses

Professional development / training

Work-life balance

Descripción de la vacante

Placements24 is seeking a dedicated and experienced Remote Clinical Research Associate (CRA) to join their expanding clinical operations team in South Africa. This fully remote role supports critical clinical trials from a home office, with strong emphasis on data integrity, site management, and regulatory compliance.

The ideal candidate has a Life Sciences background, 3+ years as a CRA, and proven expertise with ICH-GCP, CTMS, and EDC systems.

Formación

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field.
• Minimum of 3 years of experience as a Clinical Research Associate (CRA).
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
• Proven experience in remote monitoring and site management.
• Strong organizational and time management skills.

Responsabilidades

• Conduct remote site monitoring activities, including source data verification and regulatory document review.
• Ensure compliance with GCP guidelines, protocols, and regulatory requirements.
• Manage assigned clinical trial sites, providing support to investigators and staff.
• Identify, evaluate, and select potential clinical trial sites.
• Track study progress, review data, and identify discrepancies or issues.
• Prepare site monitoring reports and communicate findings to the clinical team.
• Facilitate study drug and supply management at trial sites.
• Participate in Investigator Meetings and training sessions.
• Maintain effective communication with internal stakeholders and external site personnel.
• Contribute to protocol development and operational planning.

Conocimientos

Remote monitoring

Site management

ICH-GCP knowledge

CTMS proficiency

EDC proficiency

Time management

Written and verbal communication

Independent remote work

Data integrity orientation

Educación

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field

Herramientas

CTMS

EDC systems

Descripción del empleo

About the Role

Our client, a rapidly growing pharmaceutical company dedicated to advancing global health through innovative research, is seeking a dedicated and experienced Remote Clinical Research Associate (CRA) to join their expanding clinical operations team. This fully remote position offers the flexibility to work from anywhere within South Africa, supporting critical clinical trials. The ideal candidate will be a highly organized and detail-oriented professional with a proven ability to manage clinical trial activities efficiently and compliantly. You will play a crucial role in ensuring the integrity and quality of trial data, site management, and adherence to regulatory requirements. This is an exceptional opportunity for a proactive CRA to contribute significantly to groundbreaking pharmaceutical research from the convenience of their home office, supporting trials that have the potential to impact millions of lives. We value autonomy, accountability, and a strong commitment to ethical research practices.

Key Responsibilities

• Conduct remote site monitoring activities, including source data verification and regulatory document review.
• Ensure compliance with Good Clinical Practice (GCP) guidelines, protocols, and relevant regulations.
• Manage assigned clinical trial sites, providing support and guidance to investigators and site staff.
• Identify, evaluate, and select potential clinical trial sites.
• Track study progress, review data, and identify any discrepancies or potential issues.
• Prepare site monitoring reports and communicate findings to the clinical team.
• Facilitate study drug and supply management at the trial sites.
• Participate in Investigator Meetings and training sessions.
• Maintain effective communication channels with internal stakeholders and external site personnel.
• Contribute to the development and implementation of clinical trial protocols and operational plans.

Requirements

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field.
• Minimum of 3 years of experience as a Clinical Research Associate, with demonstrated success in monitoring clinical trials.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Proven experience in remote monitoring and site management.
• Excellent organizational and time management skills, with the ability to manage multiple tasks and priorities.
• Strong written and verbal communication skills, with the ability to effectively communicate complex information.
• Proficiency in clinical trial management software (CTMS) and electronic data capture (EDC) systems.
• Ability to work independently and as part of a remote team.
• Detail-oriented with a strong commitment to data accuracy and integrity.
• Willingness to travel occasionally for essential site visits or team meetings, if required.

Benefits

This fully remote position offers significant flexibility and autonomy. Our client provides a competitive salary commensurate with experience and a comprehensive benefits package. This includes medical aid contributions, performance bonuses, and opportunities for professional development through training and certification programs. You will be part of a supportive and collaborative remote team, contributing to impactful pharmaceutical research. Enjoy the work-life balance afforded by a remote role while advancing your career in clinical research. Our client is committed to employee well-being and professional growth, offering a stimulating and rewarding work environment.