Mid Level Clinical Research Technician Jobs
Mid level clinical research technician jobs go to professionals ready to own protocol execution, mentor junior staff, and troubleshoot complex study procedures with minimal oversight. Hiring runs across Education, Healthcare & Medical Services, and Consulting & Professional Services, with 31% remote or hybrid availability, and employers like Thermo Fisher Scientific, Worldwide Clinical Trials, and Emory University competing for clinical research technicians at this level now.
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Showing 5 of 93+ Mid Level Clinical Research Technician jobs
Description
Job Summary
Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts the day-to-day activities of a research study. In general, the SCRC ensures the study maintains accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements. Beyond administrative duties, responsibilities of a SCRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities. Additionally, the SCRC will help train and mentor junior Clinical Trial Office staff.
Job Specific Duties
- Assists management with business development efforts.
- Attends and participates in investigator meetings, pre-study visits, and initiation meetings or coordinator meetings as appropriate.
- Collects and maintains accurate patient data for submission to Sponsor, maintaining proper patient records, coordinating the collection, and shipments of specimens as required by protocol.
- Communicates study objectives/procedures to relevant hospital units involved with the study including the establishment of good rapport with the Principal Investigator & providing required assistance.
- Communicates with the Sponsor or their representatives. Schedules & facilitates study monitor visits and facilitates communication between Principal Investigator and Sponsor or Sponsor’s Representatives.
- Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff.
- Interacts with patients and families to recruit study subjects and ensures compliance with the protocol.
- Responsible for speedy and adequate patient enrollment as determined by Research Management in all assigned studies.
- Demonstrates and utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol.
- Follows NCRI’s Standard Operating Procedures, AAHRPP, HIPAA, and FDA guidelines for clinical research, and keeps updated in those procedures and/or guidelines.
- Enters required data into CTMS.
- Provides new Protocols, Amendments, and study status updates to necessary research staff for digitization/entry into CTMS.
- Assists with training initiatives (including mentoring) with new and junior research staff (Research Assistants, Data Assistants and Research Volunteers).
- Keeps electronic patient files and required documents up-to-date within e-regulatory system.
- Works adjusted hours to accommodate subject visits as needed.
- Works on clinical trials, interventional studies all phases.
- Collaborates with study investigators to screen and recruit patients to available clinical trials.
Qualifications
Minimum Job Requirements
- Bachelor's degree and 3.5 years of research experience (OR) Associate's degree and 6 years of research experience (OR) 7 years of research experience
Knowledge, Skills, and Abilities
- Experience in pediatric clinical research in a hospital setting.
- Clinical research certification (CCRC, CCRP, CRA) and IATA certification.
- 5+ years research or Clinical Research Experience preferred.
- Experience with interventional (PI Initiated, IND and/or Device) clinical trials.
- Experience working on clinical trials, interventional studies all phases.
- Bilingual in English/Spanish.
- Excellent communication skills in working with both children and adults.
- Excellent organizational skills, detail-oriented, people-oriented, flexible, and adaptable to change.
- Excellent time management skills.
- Knowledge of protocols and its process.
- Experience with software applications including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment.
- Experience with relevant hospital equipment for each clinical trial project.
- Availability to work adjusted hours to accommodate subject visits.
Job:
Professional
Department:
RI - CANCER CENTER-2100-380053
Job Status:
Professional
Description
Job Summary
Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts the day-to-day activities of a research study. In general, the SCRC ensures the study maintains accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements. Beyond administrative duties, responsibilities of a SCRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities. Additionally, the SCRC will help train and mentor junior Clinical Trial Office staff.
Job Specific Duties
- Assists management with business development efforts.
- Attends and participates in investigator meetings, pre-study visits, and initiation meetings or coordinator meetings as appropriate.
- Collects and maintains accurate patient data for submission to Sponsor, maintaining proper patient records, coordinating the collection, and shipments of specimens as required by protocol.
- Communicates study objectives/procedures to relevant hospital units involved with the study including the establishment of good rapport with the Principal Investigator & providing required assistance.
- Communicates with the Sponsor or their representatives. Schedules & facilitates study monitor visits and facilitates communication between Principal Investigator and Sponsor or Sponsor’s Representatives.
- Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff.
- Interacts with patients and families to recruit study subjects and ensures compliance with the protocol.
- Responsible for speedy and adequate patient enrollment as determined by Research Management in all assigned studies.
- Demonstrates and utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol.
- Follows NCRI’s Standard Operating Procedures, AAHRPP, HIPAA, and FDA guidelines for clinical research, and keeps updated in those procedures and/or guidelines.
- Enters required data into CTMS.
- Provides new Protocols, Amendments, and study status updates to necessary research staff for digitization/entry into CTMS.
- Assists with training initiatives (including mentoring) with new and junior research staff (Research Assistants, Data Assistants and Research Volunteers).
- Keeps electronic patient files and required documents up-to-date within e-regulatory system.
- Works adjusted hours to accommodate subject visits as needed.
- Works on clinical trials, interventional studies all phases.
- Collaborates with study investigators to screen and recruit patients to available clinical trials.
Qualifications
Minimum Job Requirements
- Bachelor's degree and 3.5 years of research experience (OR) Associate's degree and 6 years of research experience (OR) 7 years of research experience
Knowledge, Skills, and Abilities
- Experience in pediatric clinical research in a hospital setting.
- Clinical research certification (CCRC, CCRP, CRA) and IATA certification.
- 5+ years research or Clinical Research Experience preferred.
- Experience with interventional (PI Initiated, IND and/or Device) clinical trials.
- Experience working on clinical trials, interventional studies all phases.
- Bilingual in English/Spanish.
- Excellent communication skills in working with both children and adults.
- Excellent organizational skills, detail-oriented, people-oriented, flexible, and adaptable to change.
- Excellent time management skills.
- Knowledge of protocols and its process.
- Experience with software applications including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment.
- Experience with relevant hospital equipment for each clinical trial project.
- Availability to work adjusted hours to accommodate subject visits.
Job:
Professional
Department:
RI - CANCER CENTER-2100-380053
Job Status:
Professional
See All 93 Mid Level Clinical Research Technician Jobs
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Find JobsMid Level Clinical Research Technician Job Market
Who's Hiring
- Thermo Fisher Scientific11
- Worldwide Clinical Trials7
- Emory University6
- University of Miami5
- UT Southwestern Medical Center4
Top Industries Hiring
- Education25
- Healthcare & Medical Services21
- Consulting & Professional Services12
- Biotechnology & Pharmaceuticals9
- Science & Research8
Mid Level Clinical Research Technician Jobs: Frequently Asked Questions
How do I get a mid level clinical research technician job?
Position yourself by highlighting hands-on experience with specific regulatory frameworks such as GCP or ICH guidelines, protocol deviations you resolved independently, and any cross-functional collaboration you led. Tailor your application to show ownership of study tasks rather than just participation. Certifications like CCRC or CCRP signal professional commitment and help your application stand out against similarly experienced candidates.
Which companies hire mid level clinical research technicians?
Companies hiring mid level clinical research technicians right now include Thermo Fisher Scientific, Worldwide Clinical Trials, and Emory University, based on current listings on Migrate Mate as of November 2026. At this experience level, hiring typically comes from contract research organizations, academic medical centers, and pharmaceutical or biotechnology companies scaling active clinical trial programs.
Are there remote mid level clinical research technician jobs?
Yes, though many roles require on-site access to study participants or lab equipment. About 31% of mid level clinical research technician openings are remote or hybrid as of November 2026, with remote work most common in data management, regulatory coordination, and monitoring roles that do not require direct specimen handling or patient contact.
How do I move up to a mid level clinical research technician role?
Progression from entry level centers on building independence across the full study lifecycle: managing your own participant visits, catching and resolving protocol deviations, and contributing to regulatory submissions. Employers promoting internally or hiring at this level look for demonstrated ownership of at least one complete study phase, improved accuracy metrics, and the ability to train newer staff on procedures.
Which industries hire the most mid level clinical research technicians?
Mid Level clinical research technician roles concentrate in Education, Healthcare & Medical Services, and Consulting & Professional Services, based on current listings on Migrate Mate as of November 2026. These sectors drive consistent demand because they operate ongoing trials, face strict regulatory timelines, and need technicians experienced enough to maintain data integrity and compliance without close supervision.