Clinical Research Coordinator

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

BLS certificate preferred

Good communication skills and English fluency will be an advantage

Benefits

You’ll work in 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

PR Newswire

Bioprocess Technology Market to Reach USD 134.06 Billion by 2035 - Credence Research

2026-10-17

Canada NewsWire

Rockwell Automation and Industry Leaders Launch the Digital CMC Consortium to Accelerate Digital Transformation in Pharmaceutical Development

2026-10-08

BioSpace

Qualifications

Bachelor's degree or equivalent and relevant formal academic / vocational qualification

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 organizational skills

Good proficiency in basic computer applications

Good interpersonal skills to work in a team environment

BLS certificate preferred

Good communication skills and 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

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

Preferred skills

BLS certificate preferred

Experience

2+ years