Clinical Research Specialist II, Peds Hematology/Oncology

University Hospitals

Clinical Research Specialist II coordinating clinical research trials in Peds Hematology/Oncology. Responsible for compliance, submission of documents, and mentoring junior staff.

Posted 5/13/2026full-timeCleveland • Ohio • 🇺🇸 United StatesJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Works with the Principal Investigator to coordinate all aspects of implementation of assigned multiple and/or complex clinical research trials.
Responsible for submission of related documents to the appropriate regulatory review committees and maintenance of regulatory files.
Performs all activities related to clinical research studies including but not limited to: screening participants for eligibility and recruitment, obtains informed consent, educates participants regarding study requirements and completes case report forms (CRF).
Responsible for in-depth knowledge of protocol requirements and Good Clinical Practice (GCP) guidelines.
Documents, records and assimilates accurate participant records and study records to ensure documentation compliance with sponsor guidelines, standard operating procedures (SOP) and internal and external regulatory agencies.
Assists with SOP, grant and protocol development and active participant in preparation of manuscripts and presentations for scientific meetings.
Establish and maintain communications with Investigator, Sponsor and internal constituents.
Mentorship of the clinical research process to the junior clinical research staff.

Requirements

What you’ll need

Bachelor's Degree (Required)
2+ years clinical research experience (Required)
Experience in a team setting (Required)
Ability to prioritize the work of multiple projects. (Required proficiency)
Knowledge of GCP and FDA guidelines. (Required proficiency)
Knowledge of Electronic Data Capture Programs. (Required proficiency)
Medical & Research Terminology. (Required proficiency)
DOT/IATA Training (Preferred proficiency)
Ability to train and mentor junior staff. (Required proficiency)
Detail-oriented person with the ability to collect, compile, and analyze information. (Required proficiency)
Ability to understand and communicate research protocol requirements to others. Able to work independently on multiple tasks and manage time effectively. (Required proficiency)
Demonstrates customer service excellence with internal and external customers (Required proficiency)
Excellent verbal, written, interpersonal and communication skills. (Required proficiency)
Computer skills (Outlook, Excel, PowerPoint, Word). (Required proficiency)
Certification in Human Subjects Protection (CITI) (Required within 30 Days)
Society of Clinical Research Associates (SoCRA) (Preferred) or ACRP Certified Professional (ACRP-CP) (Preferred)

Benefits

Comp & perks

Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients.
Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical research experienceGood Clinical Practice (GCP)FDA guidelinesElectronic Data Capture ProgramsMedical terminologyResearch terminologydata analysisprotocol developmentcase report forms (CRF)documentation compliance

Soft Skills

ability to prioritizementorshipdetail-orientedcommunication skillscustomer service excellenceteamworkindependent worktime managementinterpersonal skillstraining ability

Certifications

Bachelor's DegreeCertification in Human Subjects Protection (CITI)Society of Clinical Research Associates (SoCRA)ACRP Certified Professional (ACRP-CP)