3 Senior Pharmaceutical Clinical Research Associate jobs in Placements24
Senior Pharmaceutical Clinical Research Associate
1500 Benoni / Remote
Placements24
Posted 9 days ago
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Job Description
About the Role Our client, a leading pharmaceutical company dedicated to advancing global health, is seeking a highly competent Senior Clinical Research Associate (CRA) to join their operations based in **Benoni, Gauteng**. This pivotal role involves monitoring clinical trial sites, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP). The Senior CRA will play a crucial part in the successful execution of clinical studies, contributing to the development of innovative therapies. This is an excellent opportunity for an experienced clinical research professional to contribute to significant advancements in medicine. The successful candidate will build strong relationships with investigators and site staff, ensuring the integrity and quality of data collected. This position requires exceptional organizational skills, attention to detail, and a thorough understanding of clinical trial management. You will be a key member of the clinical operations team, ensuring the safety of trial participants and the reliability of study results. The ideal candidate is proactive, possesses strong communication skills, and is passionate about contributing to cutting-edge pharmaceutical research. This role offers a dynamic work environment with opportunities for professional growth and impact. Key Responsibilities
- Conduct site initiation, monitoring, and close-out visits for clinical trials according to protocol and GCP guidelines.
- Ensure sites are adequately trained on study protocols, procedures, and regulatory requirements.
- Verify the accuracy, completeness, and timeliness of clinical trial data through source document verification.
- Identify and resolve site-level issues, escalating critical issues to project management as needed.
- Monitor site compliance with the investigational plan, regulatory requirements, and company SOPs.
- Manage relationships with investigators and site staff, providing support and guidance.
- Prepare and submit visit reports and other required documentation in a timely manner.
- Participate in the selection and qualification of potential clinical trial sites.
- Ensure all safety reporting requirements are met by the study sites.
- Contribute to the continuous improvement of clinical trial processes and procedures.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Strong understanding of clinical trial protocols, case report forms (CRFs), and electronic data capture (EDC) systems.
- Excellent monitoring and auditing skills, with meticulous attention to detail.
- Exceptional interpersonal, communication, and negotiation skills.
- Ability to manage multiple sites and travel as required (approximately 50-60%).
- Proficiency in clinical trial management software.
- Must be legally authorized to work in **South Africa**.
- Competitive salary commensurate with experience.
- Comprehensive medical and retirement benefits.
- Allowance for travel expenses and accommodation.
- Opportunities for professional development and career advancement.
- Exposure to cutting-edge clinical trials and therapies.
- A collaborative and supportive team environment.
- Work for a company committed to improving global health outcomes.
- Employee assistance program.
- Flexible working arrangements (Hybrid).
- Significant impact on the development of new medicines.
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Senior Pharmaceutical Clinical Research Associate
0699 Polokwane / Remote
Placements24
Posted 9 days ago
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Job Description
About the Role Our client, a leading global pharmaceutical company, is looking for a dedicated and experienced Senior Clinical Research Associate (CRA) to join their team. This hybrid role will involve a mix of remote work and on-site visits to clinical trial sites, primarily in and around **Polokwane, Limpopo**. As a Senior CRA, you will be responsible for monitoring and managing clinical trial sites to ensure data accuracy, patient safety, and adherence to protocol, regulatory requirements, and Good Clinical Practice (GCP). You will play a pivotal role in the successful execution of clinical trials, contributing directly to the development of innovative therapies. This position offers an excellent opportunity to advance your career in clinical research within a dynamic and supportive environment in **Polokwane**. We seek a proactive professional with strong organizational and communication skills, capable of managing multiple responsibilities effectively. Key Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits for clinical trial sites in accordance with study protocols and GCP guidelines.
- Ensure the quality, integrity, and accuracy of data collected at clinical trial sites through source data verification.
- Monitor patient safety and adherence to the study protocol, identifying and reporting adverse events and protocol deviations.
- Manage communication between clinical trial sites, the study team, and external vendors.
- Oversee site compliance with regulatory requirements, ethical standards, and company policies.
- Train and support site staff on study-specific procedures and regulatory requirements.
- Maintain accurate and up-to-date site-related documentation and databases.
- Identify potential risks and develop mitigation strategies for assigned clinical trial sites.
- Contribute to the development and review of study-related documents, such as protocols, informed consent forms, and monitoring plans.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in monitoring clinical trial sites and performing source data verification.
- Excellent understanding of clinical trial processes and documentation.
- Strong interpersonal and communication skills, with the ability to build effective relationships with site personnel.
- Excellent organizational and time management skills, with the ability to manage multiple priorities and meet deadlines.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel to clinical trial sites, up to 60% of the time, including within the **Polokwane** region and potentially beyond.
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1
Senior Pharmaceutical Clinical Research Associate
8800 Upington
Placements24
Posted 9 days ago
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Job Description
About the Role Our client, a leading contract research organization (CRO) specializing in pharmaceuticals, is seeking an experienced and dedicated Senior Pharmaceutical Clinical Research Associate (CRA) to oversee clinical trials in the **Upington, Northern Cape** region. This critical role involves monitoring clinical trial sites, ensuring adherence to protocols, ethical standards, and regulatory requirements (e.g., ICH-GCP). You will be responsible for site initiation, monitoring patient recruitment, data verification, and ensuring the safety and well-being of trial participants. A proven track record in clinical monitoring, excellent communication skills, and a thorough understanding of clinical trial processes are essential. This position offers a unique opportunity to contribute to groundbreaking medical research in a challenging yet rewarding field. The **Upington, Northern Cape** location provides an exciting context for clinical operations. Our client is dedicated to providing comprehensive training, professional development, and career advancement opportunities for their CRAs, supporting them in delivering high-quality clinical trial oversight.
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