Clinical Trial Coordinator
Behavioral Health Market Context
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Benefits
As a W2 consultant, you will enjoy a competitive hourly rate along with a robust benefits package, including Medical, Dental, Vision insurance, a 401k plan with company matching, and life insuranceAs a W2 employee of Eliassen Group, you will be eligible for benefits such as medical, dental, vision, and more, if you work 30 or more hours per weekRefer a candidate to our team, and you may be eligible for a $1,000 referral bonus!
Job Description
Clinical Trial Coordinator
We are seeking a dedicated Clinical Trial Coordinator to join our team and support clinical trial activities across various studies. This is a fantastic opportunity for individuals who are passionate about advancing drug development and ensuring successful trial execution.
Your primary responsibilities will include tracking operational activities, maintaining essential study documentation such as the electronic Trial Master File (eTMF), and collaborating with internal teams, CROs, vendors, and clinical sites. Reporting to the Clinical Operations Head, you will play a crucial role in our cross-functional efforts to streamline clinical operations.
As a W2 consultant, you will enjoy a competitive hourly rate along with a robust benefits package, including Medical, Dental, Vision insurance, a 401k plan with company matching, and life insurance.
Responsibilities:
• Assist Clinical Operations Leads and Trial Managers with day-to-day trial operations, ensuring compliance with SOPs and regulatory guidelines.
• Maintain clinical trial documentation, including the eTMF, while managing project processes and tracking systems.
• Work with Clinical Sample Management to coordinate biomarker testing with third-party laboratories.
• Collaborate with Clinical Data Management to facilitate timely training and access for external stakeholders across various platforms such as EDC, IWRS, ePRO, and eTMF.
• Organize project team and departmental meetings, including preparation and maintenance of related documentation.
• Assist with vendor and clinical site agreements, budgets, and the tracking of purchase orders and invoices.
• Develop and maintain strong relationships with stakeholders at our client, CRO partners, and clinical sites.
Experience Requirements:
• Minimum of 2 years of experience in a clinical research environment.
• Basic knowledge of drug development and familiarity with FDA and ICH GCP guidelines.
• Strong verbal and written communication skills.
• Excellent organizational skills and attention to detail.
• Able to learn quickly, take direction, and manage multiple tasks effectively.
• Self-motivated and adaptable in a dynamic work environment.
Education Requirements:
• Bachelor's degree in a science-related discipline preferred.
Eliassen Group promotes transparency in hiring processes. We utilize AI tools for initial application screening, and you may receive notifications from our virtual recruiting team regarding steps in the application process.
As a W2 employee of Eliassen Group, you will be eligible for benefits such as medical, dental, vision, and more, if you work 30 or more hours per week.
Eliassen Group is an Equal Opportunity Employer, committed to building a diverse team. All employment decisions are based on merit and business needs.
Refer a candidate to our team, and you may be eligible for a $1,000 referral bonus!
We are seeking a dedicated Clinical Trial Coordinator to join our team and support clinical trial activities across various studies. This is a fantastic opportunity for individuals who are passionate about advancing drug development and ensuring successful trial execution.
Your primary responsibilities will include tracking operational activities, maintaining essential study documentation such as the electronic Trial Master File (eTMF), and collaborating with internal teams, CROs, vendors, and clinical sites. Reporting to the Clinical Operations Head, you will play a crucial role in our cross-functional efforts to streamline clinical operations.
As a W2 consultant, you will enjoy a competitive hourly rate along with a robust benefits package, including Medical, Dental, Vision insurance, a 401k plan with company matching, and life insurance.
Responsibilities:
• Assist Clinical Operations Leads and Trial Managers with day-to-day trial operations, ensuring compliance with SOPs and regulatory guidelines.
• Maintain clinical trial documentation, including the eTMF, while managing project processes and tracking systems.
• Work with Clinical Sample Management to coordinate biomarker testing with third-party laboratories.
• Collaborate with Clinical Data Management to facilitate timely training and access for external stakeholders across various platforms such as EDC, IWRS, ePRO, and eTMF.
• Organize project team and departmental meetings, including preparation and maintenance of related documentation.
• Assist with vendor and clinical site agreements, budgets, and the tracking of purchase orders and invoices.
• Develop and maintain strong relationships with stakeholders at our client, CRO partners, and clinical sites.
Experience Requirements:
• Minimum of 2 years of experience in a clinical research environment.
• Basic knowledge of drug development and familiarity with FDA and ICH GCP guidelines.
• Strong verbal and written communication skills.
• Excellent organizational skills and attention to detail.
• Able to learn quickly, take direction, and manage multiple tasks effectively.
• Self-motivated and adaptable in a dynamic work environment.
Education Requirements:
• Bachelor's degree in a science-related discipline preferred.
Eliassen Group promotes transparency in hiring processes. We utilize AI tools for initial application screening, and you may receive notifications from our virtual recruiting team regarding steps in the application process.
As a W2 employee of Eliassen Group, you will be eligible for benefits such as medical, dental, vision, and more, if you work 30 or more hours per week.
Eliassen Group is an Equal Opportunity Employer, committed to building a diverse team. All employment decisions are based on merit and business needs.
Refer a candidate to our team, and you may be eligible for a $1,000 referral bonus!
Qualifications
- •Minimum of 2 years of experience in a clinical research environment
- •Basic knowledge of drug development and familiarity with FDA and ICH GCP guidelines
- •Strong verbal and written communication skills
- •Excellent organizational skills and attention to detail
- •Able to learn quickly, take direction, and manage multiple tasks effectively
- •Self-motivated and adaptable in a dynamic work environment
Responsibilities
- •We are seeking a dedicated Clinical Trial Coordinator to join our team and support clinical trial activities across various studies
- •This is a fantastic opportunity for individuals who are passionate about advancing drug development and ensuring successful trial execution
- •Your primary responsibilities will include tracking operational activities, maintaining essential study documentation such as the electronic Trial Master File (eTMF), and collaborating with internal teams, CROs, vendors, and clinical sites
- •Reporting to the Clinical Operations Head, you will play a crucial role in our cross-functional efforts to streamline clinical operations
- •Assist Clinical Operations Leads and Trial Managers with day-to-day trial operations, ensuring compliance with SOPs and regulatory guidelines
- •Maintain clinical trial documentation, including the eTMF, while managing project processes and tracking systems
- •Work with Clinical Sample Management to coordinate biomarker testing with third-party laboratories
- •Collaborate with Clinical Data Management to facilitate timely training and access for external stakeholders across various platforms such as EDC, IWRS, ePRO, and eTMF
- •Organize project team and departmental meetings, including preparation and maintenance of related documentation
- •Assist with vendor and clinical site agreements, budgets, and the tracking of purchase orders and invoices
- •Develop and maintain strong relationships with stakeholders at our client, CRO partners, and clinical sites
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