Medical Study Coordinator

Key Responsibilities:

• Safeguarding the wellbeing of research subjects in a medical capacity, ensuring that all procedures are conducted with the highest standards of care and safety.
• Reviewing study protocols and executing procedures in alignment with protocols and regulatory, health, and safety standards, ensuring compliance with all relevant guidelines and regulations.
• Recruiting and coordinating communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study.
• Following applicable regulations globally and by region, ensuring that all activities are conducted in accordance with local and international standards.
• Collaborating with cross-functional teams to develop study materials, including informed consent forms, study manuals, and other essential documents.
• Monitoring trial progress and addressing any issues that arise during the study, ensuring that all problems are promptly identified and resolved.
• Providing organizational related support or service, typically under supervision, assisting with administrative tasks and other support activities as needed.
• Performing routine tasks with some deviation from standard practice, adapting to changing circumstances and requirements as necessary.
• Utilizing broad knowledge of operational systems and practices gained through extensive experience and/or education, applying this knowledge to improve study processes and outcomes.
• Qualifications:
• A high school diploma or equivalent is required.
• An Associate's degree or higher in a related field is preferred.
• Minimum of 2 years of experience in clinical operations or a related field.
• Strong understanding of clinical research protocols and regulatory requirements.
• Certifications:
• CCRC (Certified Clinical Research Coordinator) or equivalent certification is preferred.
• BLS (Basic Life Support) certification is required.
• Necessary Skills:
• Excellent communication and interpersonal skills.
• Strong organizational and time management abilities.
• Attention to detail and accuracy in documentation.
• Ability to work effectively in a team environment.
• Proficiency in Microsoft Office Suite and clinical trial management software.
• Why Join Us:
• Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA-approved drugs.

As a Clinical Operations Specialist, you will play a critical role in ensuring the success of our clinical trials. Your primary responsibility will be to safeguard the wellbeing of research subjects in a medical capacity, ensuring that all procedures are conducted with the highest standards of care and safety.

We are seeking an experienced and highly skilled individual who can collaborate with cross-functional teams to develop study materials, including informed consent forms, study manuals, and other essential documents. You will also be responsible for monitoring trial progress and addressing any issues that arise during the study.

If you are a motivated and detail-oriented individual with excellent communication and interpersonal skills, we encourage you to apply for this exciting opportunity.

At our organization, we value teamwork and collaboration. As a Clinical Operations Specialist, you will have the opportunity to work closely with our cross-functional teams to achieve common goals.

Our organization is committed to providing a safe and healthy work environment for all employees. We offer competitive compensation and benefits packages, as well as opportunities for professional growth and development.

Thank you for considering this opportunity. We look forward to reviewing your application.

For more information about our organization, please visit our website.