Pharmaceutical Clinical Research Associate (CRA)

Placements24; Mbombela (Nelspruit); Hybrid; ZAR 700,000 - 1,000,000; Full time

Benefits offered by this job

Hybrid work

Travel reimbursement

Health benefits

Dental/ Vision coverage

Job summary

Placements24 seeks a dedicated Pharmaceutical Clinical Research Associate (CRA) to support trials around Nelspruit. The role blends field site monitoring with remote administrative duties, ensuring data integrity and patient safety across studies.

The ideal candidate has a life sciences background and at least 3 years of CRA experience, with strong knowledge of GCP and regulations. Travel to sites is required in a hybrid work setup near Nelspruit.

Qualifications

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3 years of CRA experience in the pharmaceutical industry.
• In-depth knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Experience in site monitoring, data verification, and regulatory compliance.
• Strong organizational and interpersonal skills.
• Ability to travel to sites as needed and work in a hybrid remote/field environment near Nelspruit.

Responsibilities

• Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements.
• Perform site initiation, interim monitoring, and close-out visits.
• Verify the accuracy and completeness of clinical data.
• Manage study supplies and investigational product accountability at sites.
• Train site personnel on study procedures and regulatory requirements.
• Act as the primary point of contact for investigative sites and resolve study-related issues.

Skills

CRA experience

GCP knowledge

Regulatory compliance

Data verification

Education

Bachelor's degree in life sciences

Tools

EDC systems

Regulatory systems

Job description

About the Role

Our client is seeking a dedicated and meticulous Pharmaceutical Clinical Research Associate (CRA) to join their team, supporting operations in and around Nelspruit . This role is essential for managing and monitoring clinical trials, ensuring data integrity, patient safety, and adherence to protocols and regulations. You will act as a vital link between investigative sites and the sponsor, conducting site visits, training staff, and overseeing study conduct. This hybrid role offers the chance to contribute to cutting-edge pharmaceutical research while maintaining a balance between field responsibilities and remote administrative tasks, ensuring the successful execution of critical clinical studies.

Key Responsibilities

• Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements
• Perform site initiation, interim monitoring, and close-out visits
• Verify the accuracy and completeness of clinical data
• Manage study supplies and investigational product accountability at sites
• Train site personnel on study procedures and regulatory requirements
• Act as the primary point of contact for investigative sites and resolve study-related issues

Requirements

• Bachelor's degree in a life science, nursing, or related field
• Minimum of 3 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical industry
• In-depth knowledge of Good Clinical Practice (GCP) and regulatory guidelines
• Experience in site monitoring, data verification, and regulatory compliance
• Strong organizational, communication, and interpersonal skills
• Ability to travel to sites as needed and work effectively in a hybrid remote/field environment based near Nelspruit

Benefits

• Competitive salary and potential for performance bonuses
• Hybrid work arrangement offering flexibility and work-life integration
• Comprehensive health, dental, and vision benefits
• Travel expenses fully reimbursed
• Opportunity to work on diverse and impactful clinical trials advancing pharmaceutical innovation