Clinical Research Coordinator II

Responsibilities

• Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines
• Provide medical care to patients, always ensuring patient safety comes first
• Schedule subject visits within protocol windows, ensuring scheduling capacity is maximized
• Perform all defined study activities (i.e., informed consent, screening, and protocol procedures which include but are not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.)
• Record all patient information and results from tests as per protocol on required forms
• Where required, may complete IP accountability logs and associated information
• Reports suspected non-compliance with relevant site staff
• Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study
• Promotes the company and builds a positive relationship with patients to ensure retention
• Attend site initiation meetings and all other relevant meetings to receive training on protocol
• May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results
• Logs/complete information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe
• Gather and maintain source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded
• Adhere to company COP/SCOP
• May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility

Preferred

• English fluency will be an advantage

Benefits

• An environment where collaboration and development are part of the everyday experience
• Glassdoor
• 3.5
• Thermo Fisher Scientific is a biotechnology and laboratory equipment company that provides a wide range of scientific products and services.
• Waltham, Massachusetts, USA
• https://www.thermofisher.com
• Public Company
• Total Funding
• $19.77B
• Key Investors
• National Grid
• 2026-02-09
• Post Ipo Debt· $3.8B
• 2025-11-24
• Post Ipo Debt· $2.42B
• 2025-09-30
• Post Ipo Debt· $2.5B
• Leadership Team
• Marc Casper
• Chairman and CEO
• Daniella Cramp
• Senior Vice President and President, Bioproduction Group
• Recent News
• GenomeWeb
• Thermo Fisher Raises 2026 Guidance, Reports 9 Percent Jump in Q3 Revenue
• 2026-10-22
• PR Newswire
• Bioprocess Technology Market to Reach USD 134.06 Billion by 2035 - Credence Research
• 2026-10-17
• Canada NewsWire

Qualifications

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• BLS certificate required
• Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years')
• In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role
• Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
• Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving
• Demonstrated ability to exercise discretion and sound judgement
• Good decision-making, negotiation and influencing skills
• Good communication skills
• Good organizational skills
• Good proficiency in basic computer applications
• Good interpersonal skills to work in a team environment
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf
• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences
• Frequently interacts with others to obtain or relate information to diverse groups
• Ability to perform under stress
• Ability to multi-task
• English fluency will be an advantage
• Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years’).

Required skills

• Basic Life Support (BLS), Clinical Research, Informed Consent, Safety Monitoring, Standard Operating Procedures (SOPs)

Preferred skills

• English fluency will be an advantage

Experience

• 2+ years