Clinical Research Associate (Pharmaceutical)

Placements24; Soweto; On-site; ZAR 420,000 - 600,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Professional development

Job summary

Placements24 is seeking a highly competent Clinical Research Associate (CRA) for operations based in Soweto, Gauteng. The role focuses on overseeing clinical trials, ensuring protocol adherence and regulatory compliance, and liaising with sites, ethics committees, and regulators.

The ideal candidate has a life sciences degree, at least 3 years of CRA experience in pharmaceutical trials, and strong organizational, communication, and data monitoring skills to support successful study execution.

Qualifications

• Bachelor's degree in a life science, nursing, pharmacy, or related field.
• Minimum of 3 years of CRA experience in pharmaceutical clinical trials.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Experience with site monitoring, data review, and regulatory inspections.
• Strong organizational skills and attention to detail; effective communication and interpersonal skills.

Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits per GCP and study protocols.
• Ensure accuracy, completeness, and integrity of clinical trial data at investigative sites.
• Verify compliance of study sites with protocols, SOPs, and regulatory requirements.
• Serve as the primary liaison between sponsor and investigative sites.
• Manage study supplies and ensure proper documentation.
• Identify and report adverse events and protocol deviations promptly.

Skills

Organizational skills

Communication skills

Attention to detail

Interpersonal skills

Regulatory knowledge

Education

Bachelor's degree in a life science, nursing, pharmacy, or a related field

Job description

About the Role

Our client is seeking a highly competent and detail-oriented Clinical Research Associate (CRA) specializing in pharmaceuticals for their operations based in Soweto . This role is crucial for overseeing and managing clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will be instrumental in the successful execution of studies that contribute to the development of new and improved medicines. The ideal candidate will possess a strong understanding of clinical trial processes, excellent organizational skills, and the ability to effectively interact with investigative sites, ethics committees, and regulatory bodies.

Key Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits for clinical trials in accordance with Good Clinical Practice (GCP) guidelines and study protocols.
• Ensure the accuracy, completeness, and integrity of clinical trial data collected at investigative sites.
• Verify compliance of study sites with protocols, Standard Operating Procedures (SOPs), and regulatory requirements.
• Serve as the primary liaison between the sponsor (our client) and the investigative sites.
• Manage study supplies, including investigational product, and ensure proper documentation is maintained.
• Identify and report adverse events and protocol deviations in a timely manner.

Requirements

• Bachelor's degree in a life science, nursing, pharmacy, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate (CRA) or equivalent role in pharmaceutical clinical trials.
• In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements for clinical research.
• Experience with site monitoring, data review, and regulatory inspections.
• Strong organizational skills, excellent attention to detail, and the ability to manage multiple priorities.
• Effective communication and interpersonal skills, with the ability to build rapport with site personnel.

Benefits

• Competitive salary and performance-based incentives.
• Comprehensive health, dental, and vision insurance plans.
• Mileage reimbursement and per diem allowances for site visits.
• Opportunities for professional development and career advancement within clinical research.
• A challenging and rewarding role contributing to groundbreaking pharmaceutical research.