Role at a glance
- Job function
-
Healthcare Healthcare Administration & Patient Services
- Salary
- Not Disclosed
- Location
- Austin, Texas, United States
- Work arrangement
- On-site
- Employment
- Full-time
- Experience
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
- Education
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
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Role Summary
The Associate Clinical Research Manager assists with managing clinical trials involving patient and healthy subject populations in inpatient and outpatient settings. The role supports study conduct and serves as a liaison between senior project team members and study subjects.
What You'll Do
- Participate with senior project team members to meet project needs, projections, and deadlines.
- Oversee the organization and accuracy of project documents.
- Work with management to understand departmental needs and improve processes.
- Support study conduct by working with the study monitor and study subjects.
- Oversee data entry, source data quality control, EDC entry and query resolution, lab data verification, and subject eligibility review...
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Bachelor's degree or equivalent and relevant formal academic / vocational qualification; previous experience comparable to 0 to 2 years. Basic knowledge of Phase I processes and clinical study operations, FDA regulations and ICH GCP guidelines, and Microsoft Office applications. Requires time management, multitasking, written and verbal communication, prioritization, adaptability, and liaison skills.
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join Us as an Associate Clinical Research Manager - Make an Impact at the Forefront of InnovationThe Associate Clinical Research Manager assists with managing various aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor, investigator and research team communications.
What You'll Do:
• Actively participate with senior project team members to meet project needs, projections and deadlines.
• Oversee organization and accuracy of project documents.
• Work with management on understanding departmental needs and improving processes.
• Provide support for the study conduct, working directly with study monitor and study subjects.
• Oversee data entry, source data QC, EDC data entry and EDC query resolution, lab data verification, subject eligibility status review and subject eligibility notification.
Education & Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
• Basic knowledge of Phase I processes and clinical study operations
• Fundamental knowledge of FDA regulations and ICH GCP guidelines
• Basic computer skills with working knowledge of Microsoft Office applications
• Time management and multi-tasking skills
• Written and verbal communication skills
• Ability to prioritize workload and adapt to changing study needs
• Ability to act as a liaison between external and internal groups.
Working Conditions and Environment:
• Work is performed in an office/ laboratory and/or a clinical environment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Exposure to electrical office equipment.
• Personal protective equipment required such as protective eyewear, garments and gloves.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.