Late Phase Clinical Research Manager Thermo Fisher Scientific - 3.4 Austin, TX Job Details Full-time 6 hours ago Qualifications Fiscal management Managing healthcare project budgets Informed consent Clinical trial risk management Mid-level Project communication management Patient safety ICH guidelines Bachelor's degree Informed consent procedures implementation Managing clinical research teams Forecasting Desktop applications Vendor relationship management Vendor communication Clinical trial standard operating procedures Implementing research protocols Communication with regulatory authorities for clinical trials Productivity software Clinical quality assurance standards Data collection Project contract management Research budget management Clinical program risk management Research and development project management Project Development Clinical consent forms Ethical review application preparation Project leadership Standard operating procedures (SOPs) Full Job Description Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Manager - Make an Impact at the Forefront of Innovation The Clinical Research Manager manages all aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. The role involves acting as liaison between functions (i.e. PM, investigator, research team, etc.) The Clinical Research Manager ensures client requirements and specifications are communicated to the research teams and any issues/questions raised by the research team or investigators are communicated back to the project leads and client (as needed) for resolution.

What You'll Do:

Serve as a primary point of contact for the project team and the business unit for clinical site related aspects of the study. Collaborate with internal departments to ensure deliverables are met as defined within the contract and study timeline. Manage all clinical and administrative aspects of a clinical project, including site level study set-up, recruitment, conduction and data collection. Manage IRB submissions including creation of study specific informed consent forms, SAE notifications and maintenance of the regulatory file and documents. Collect feedback from various departments to create a risk register for each study and maintains and updates the register throughout the study. Work with the Principal Investigator to ensure that a risk mitigation plan (RMP) is finalized and reviewed by the safety committee prior to study conduct. Work closely with finance department to manage fiscal aspects of study conduct while meeting sponsor requirements and adhering to the protocol, SOPs and contract. Provide vendor oversight when services are contracted.

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 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:

Knowledge of Phase I processes and strong knowledge of clinical study operations Knowledge of FDA regulations and ICH GCP guidelines Solid computer skills with working knowledge of Microsoft Office applications Good time management and multi-tasking skills Solid written and verbal communication skills Strong organizational and prioritization skills with the ability to prioritize workload and adapt to changing study needs Favorable consulting skills with t to act as a liaison between external and internal groups Knowledge of budgeting/forecasting/planning projects.

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.