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Clinical Research Coordinator III - RN, Part-Time

Thermo Fisher Scientific

Clinical Research Coordinator III - RN, Part-Time

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

Discover Impactful Work:

We are seeking a Clinical Research Coordinator III (Registered Nurse) to support our government customer on-site in Silver Spring, Maryland.  This is a part-time position with availability needed from 6:00 am - 10: 00 am. Successful candidates must be experienced with vaccine preparation and administration.

  • Relocation assistance is NOT provided for this role.
  • Must be a U.S. citizen.
  • Must be able to pass a comprehensive background check, which includes a drug screening and a physical. 
  • Required to be a Registered Nurse licensed to practice in the state of Maryland.

A day in the Life:

  • Organizes and prioritizes all activities associated with conducting phase 1, 2, and 3 clinical and operational research studies within a military clinic setting.
  • Reviews and understands research protocols, ensuring applicable regulations and guidelines are followed.
  • Organizes research information for clinical projects
  • Selects and observes subjects and assists with data analysis and reporting.
  • Oversees experiment scheduling and collection of data.
  • Participates in source document and study document design, writing SSP, materials planning, visit schedule creation, etc.
  • Enters required data routinely on CRFs and audit records for accuracy, resolve discrepancies, and correct as necessary.
  • Maintains study/test article or investigational product accountability and administration.
  • Monitors study data collection procedures to ensure uniformly high levels of compliance with GCP, GLP, FDA and other government- or locally required guidance.
  • Relies on experience and judgment to plan and accomplish goals. Works under general supervision and performs a variety of tasks.

Keys to Success:

Required Education

  • Required to be a Registered Nurse licensed to practice in the state of Maryland, who is skilled and qualified in nursing procedures to include, but not limited to the administration of experimental vaccines and other parenteral therapeutics as per specific protocol guidance in accordance with the 21 Code of Federal Regulation (CFR) 11, 50, 54, 56, 312, and 314.
  • Basic Life Support (BLS –CPR/AED) certification.

Required Experience and Skills:

  • Five (5) years of experience in clinical research coordination, with expertise in FDA-regulated trials.  
  • Experience utilizing clinical trial management systems and databases (e.g., REDcap and Inform).
  • Must be able to work both independently and in a team setting following a brief period of specific technical training.
  • Must have excellent communication, organization, and prioritization skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers and customers.
  • Maintenance of Certification in Clinical Research Coordination by Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA).

Desired Experience and Skills

  • Advanced Cardiac Life Support (ACLS) certification encouraged.
  • Certification in clinical research (e.g., CCRP or CCRA) is preferred.
  • Commission for Case Manager Certification (CCMC) certification preferred.


Working Conditions and Environment:
• Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions

Compensation and Benefits

The salary pay range estimated for this position CRA (Level II) based in Maryland is $38.46–$44.23.

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. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • 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, and 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

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Locations

  • Rockville, Maryland, United States of America

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Clinical research coordinationintermediate
  • Vaccine preparation and administrationintermediate
  • FDA-regulated trialsintermediate
  • Clinical trial management systems (e.g., REDcap, Inform)intermediate
  • Data analysis and reportingintermediate
  • GCP, GLP complianceintermediate

Required Qualifications

  • Registered Nurse licensed in Maryland (experience)
  • 5 years clinical research coordination experience (experience)
  • Basic Life Support (BLS-CPR/AED) certification (experience)
  • U.S. citizen (experience)
  • Pass background check, drug screening, physical (experience)

Responsibilities

  • Organize and prioritize clinical research activities
  • Review research protocols and ensure regulatory compliance
  • Select and observe subjects
  • Oversee experiment scheduling and data collection
  • Enter data on CRFs and audit records
  • Maintain study product accountability
  • Monitor data collection for compliance

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Thermo Fisher Scientific logo

Clinical Research Coordinator III - RN, Part-Time

Thermo Fisher Scientific

Clinical Research Coordinator III - RN, Part-Time

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

Discover Impactful Work:

We are seeking a Clinical Research Coordinator III (Registered Nurse) to support our government customer on-site in Silver Spring, Maryland.  This is a part-time position with availability needed from 6:00 am - 10: 00 am. Successful candidates must be experienced with vaccine preparation and administration.

  • Relocation assistance is NOT provided for this role.
  • Must be a U.S. citizen.
  • Must be able to pass a comprehensive background check, which includes a drug screening and a physical. 
  • Required to be a Registered Nurse licensed to practice in the state of Maryland.

A day in the Life:

  • Organizes and prioritizes all activities associated with conducting phase 1, 2, and 3 clinical and operational research studies within a military clinic setting.
  • Reviews and understands research protocols, ensuring applicable regulations and guidelines are followed.
  • Organizes research information for clinical projects
  • Selects and observes subjects and assists with data analysis and reporting.
  • Oversees experiment scheduling and collection of data.
  • Participates in source document and study document design, writing SSP, materials planning, visit schedule creation, etc.
  • Enters required data routinely on CRFs and audit records for accuracy, resolve discrepancies, and correct as necessary.
  • Maintains study/test article or investigational product accountability and administration.
  • Monitors study data collection procedures to ensure uniformly high levels of compliance with GCP, GLP, FDA and other government- or locally required guidance.
  • Relies on experience and judgment to plan and accomplish goals. Works under general supervision and performs a variety of tasks.

Keys to Success:

Required Education

  • Required to be a Registered Nurse licensed to practice in the state of Maryland, who is skilled and qualified in nursing procedures to include, but not limited to the administration of experimental vaccines and other parenteral therapeutics as per specific protocol guidance in accordance with the 21 Code of Federal Regulation (CFR) 11, 50, 54, 56, 312, and 314.
  • Basic Life Support (BLS –CPR/AED) certification.

Required Experience and Skills:

  • Five (5) years of experience in clinical research coordination, with expertise in FDA-regulated trials.  
  • Experience utilizing clinical trial management systems and databases (e.g., REDcap and Inform).
  • Must be able to work both independently and in a team setting following a brief period of specific technical training.
  • Must have excellent communication, organization, and prioritization skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers and customers.
  • Maintenance of Certification in Clinical Research Coordination by Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA).

Desired Experience and Skills

  • Advanced Cardiac Life Support (ACLS) certification encouraged.
  • Certification in clinical research (e.g., CCRP or CCRA) is preferred.
  • Commission for Case Manager Certification (CCMC) certification preferred.


Working Conditions and Environment:
• Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions

Compensation and Benefits

The salary pay range estimated for this position CRA (Level II) based in Maryland is $38.46–$44.23.

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. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • 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, and 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

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Locations

  • Rockville, Maryland, United States of America

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Clinical research coordinationintermediate
  • Vaccine preparation and administrationintermediate
  • FDA-regulated trialsintermediate
  • Clinical trial management systems (e.g., REDcap, Inform)intermediate
  • Data analysis and reportingintermediate
  • GCP, GLP complianceintermediate

Required Qualifications

  • Registered Nurse licensed in Maryland (experience)
  • 5 years clinical research coordination experience (experience)
  • Basic Life Support (BLS-CPR/AED) certification (experience)
  • U.S. citizen (experience)
  • Pass background check, drug screening, physical (experience)

Responsibilities

  • Organize and prioritize clinical research activities
  • Review research protocols and ensure regulatory compliance
  • Select and observe subjects
  • Oversee experiment scheduling and data collection
  • Enter data on CRFs and audit records
  • Maintain study product accountability
  • Monitor data collection for compliance

Target Your Resume for "Clinical Research Coordinator III - RN, Part-Time" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Clinical Research Coordinator III - RN, Part-Time. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Clinical Research Coordinator III - RN, Part-Time" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Clinical Research Coordinator III - RN, Part-Time @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.