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Syneos Health, Inc.; Gauteng; Remote; ZAR 1 016 000 - 1 356 000; Full time

Job summary

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate to conduct on-site and remote monitoring of clinical studies. The ideal candidate will have a Bachelor’s degree and 2-4 years of experience in clinical research monitoring, with strong knowledge of Good Clinical Practice. Responsibilities include developing monitoring tools, ensuring compliance, and collaborating with cross-functional teams. This position offers an opportunity to contribute to essential clinical trials in a supportive work culture.

Qualifications

• Minimum of 2-4 years of experience in clinical research monitoring.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Excellent communication and interpersonal skills.

Responsibilities

• Conduct on-site and remote monitoring of clinical research studies.
• Develop and implement tools and procedures for quality monitoring.
• Collaborate with cross-functional teams to support clinical trial operations.

Skills

Attention to detail

Analytical skills

Problem-solving abilities

Effective teamwork

Organizational skills

Education

Bachelor’s degree in a related field

Tools

Clinical trial management systems

Microsoft Office Suite

Job description

Overview

Updated: September 18,

Location: ZAF-Remote

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you\u2019ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29, employees, across countries already know: WORK HERE MATTERS EVERYWHERE

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.

We are committed to our Total Self culture 20r where you can authentically be yourself.

Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.

We are continuously building the company we all want to work for and our customers want to work with.

Job Responsibilities

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
• Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
• Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
• Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues
• Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans
• Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

Qualifications

• Bachelor\u2019s degree in a related field or equivalent experience
• Minimum of 2-4 years of experience in clinical research monitoring
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
• Excellent communication and interpersonal skills
• Ability to work independently and manage multiple priorities
• Proficiency in using clinical trial management systems and other relevant software

Certifications

• Certified Clinical Research Associate (CCRA) or equivalent certification preferred

Necessary Skills

• Attention to detail and strong analytical skills
• Problem-solving abilities and critical thinking
• Ability to work effectively in a team environment
• Strong organizational and time management skills
• Proficiency in Microsoft Office Suite

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over Studies across 73, Sites and ,+ Trial patients.

No matter what your role is, you\u2019ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.

Learn more about Syneos Health.

Additional information: This description includes standard boilerplate language regarding duties, at-will employment, equal opportunity, accessibility, and other legal disclosures. It is not intended to modify the terms of any employment agreement.

Summary

Roles within Clinical Monitoring / CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring.

These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Impact and Contribution: Roles have a significant impact on the quality and integrity of clinical research studies, contributing to reliability and validity of study results and enhancing the efficiency and effectiveness of clinical trials.

At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn\u2019t align perfectly, we encourage you to apply anyway. We also encourage joining our Talent Network to stay connected to additional career opportunities.

Syneos Health (Nasdaq: SYNH) is a leading integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. We support a diverse, equitable and inclusive culture.

Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status.

If you require reasonable accommodation to complete any part of the application process, please contact us at #J-