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

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.)

Phlebotomy and sample processing/shipping

Record all patient information and results from tests as per protocol on required forms

Where required, may complete IP accountability logs and associated information

Report suspected of non-compliance to relevant site staff

Ensure that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study

Promote the company and build 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

Log/complete information on sponsor systems and ensure all information provided is accurate (i.e., case report forms, EDC, etc.) and ensure it is completed within timeframe

Gather source documents, update 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

Benefits

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.

A choice of national medical and dental plans, and a national vision plan, including health incentive programs

Employee assistance and family support programs, including commuter benefits and tuition reimbursement

At least 120 hours paid time off (PTO)

10 paid holidays annually

Paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave)

Accident and life insurance

Short- and long-term disability in accordance with company policy

Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

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

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Customer Service and Support

Engineering and Development

Management and Executive

Product Management

Accounting and Finance

Marketing

Sales

Legal and Compliance

Human Resources

Arts and Entertainment

Creatives and Design

Trends of Total Sponsorships

*2026

Qualifications

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification in the clinical / medical field
• BLS certificate required
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 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

• Basic 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
• Adequate decision-making, negotiation and influencing skills
• Decent communication skills and English fluency will be an advantage
• Decent organizational skills
• Essential proficiency in basic computer applications
• Decent interpersonal skills to work in a team environment
• Occasional travel may be domestic or international
• Ability to work in an upright and /or stationary position for 6-8 hours per day
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists
• Frequent mobility required
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs
• 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
• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task
• Regular and consistent attendance
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’).

Required skills

Clinical Research, Clinical Practice (GCP), Standard Operating Procedures (SOPs), Informed Consent Administration, Patient Safety Monitoring, BLS Certification

Experience

Entry level