Research Coordinator II - Academic Offices of Clinical Trials

Research Coordinator II - Academic Offices of Clinical Trials jobs in United States

Tags

25+ applicants

Original Job Post

Houston Methodist

80

GOOD MATCH

Experience Level

91

Skill

65

Industry Exp.

81

Health Care

Responsibilities

Under the direction of the Principal Investigator (PI), drafts various communications with the Sponsor and/or regulatory documents to be sent to the Sponsor

Identifies and recruits clinical research subjects and monitors enrollment goals

May conduct in-services to floor nurses/physicians; assists in precepting new clinical research staff and educating other research staff regarding scientific aspects of studies

Teaches peers to critically think by verbally expressing rationale for decisions and follows up consistently. Uses peer-to-peer accountability towards improvement of department score for turnover/retention/employee engagement

Participates in the Principal Investigator (PI) meetings

Schedules, coordinates, and participates in the pre-site visit and site initiation visits; coordinates study initiation. Obtains Informed Consent from study participant and documents appropriately

Obtains vital signs and performs phlebotomy per training and competence; monitors participants’ labs and notifies the PI of laboratory findings

Prepares Institutional Research Board (IRB) documents under the direction of the PI, assists with answering IRB stipulations to obtain final approval; documents IRB approval and contract approval

Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process. Adheres to internal controls established for the department

Assists with the budget development and Medicare coverage analysis

Utilizes resources effectively and efficiently, demonstrating responsible financial stewardship. Manages own time effectively and prioritizes work to achieve maximum results in a timely manner

Assists PI and/or research nurse in the planning and design of source documents for protocol

Assists in developing procedures for laboratory collection and storage

Incorporates directions from other health care disciplines into clinical research protocols when reviewing patient eligibility; assists in eliciting relevant data from sources outside of the hospital

Proactively manages own professional development and completes My Development Plan

Preferred

CCRC - Certified Clinical Research Coordinator (ACRP)

CCRP - Certified Clinical Research Professional (SOCRA)

Glassdoor

4.1

Academic health system and hospital network.

Houston, Texas, USA

http://www.houstonmethodist.org/

Late Stage

Leadership Team

Jenny Chang

President and CEO, Houston Methodist Academic Institute and EVP and Chief Academic Officer, HM

Roberta Schwartz

EVP and Chief Innovation Officer

Recent News

PR Newswire

Twelve U.S. Health Systems and Aidoc Unite to Confront America's Diagnostic Capacity Crisis

2026-08-11

New Peer-Reviewed Research Provides First Independent Evidence That Ambient AI Increases Surgical Case Volume

2026-08-05

American Hospital Association

Qualifications

Bachelor's degree

Four years of research experience

Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going skills, competency assessments, and performance evaluations

Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security

Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles

Ability to work independently

Capable of handling challenging/difficult situations

Demonstrates sound judgment and executes above average analytical skills

CCRC - Certified Clinical Research Coordinator (ACRP)

CCRP - Certified Clinical Research Professional (SOCRA)

Required skills

Clinical Research Coordination, Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), Informed Consent Documentation, Phlebotomy, Institutional Research Board (IRB) Documentation, Budget Development, Medicare Coverage Analysis

Preferred skills

CCRC - Certified Clinical Research Coordinator (ACRP), CCRP - Certified Clinical Research Professional (SOCRA), Glassdoor, 4.1, Academic health system and hospital network., Houston, Texas, USA, http://www.houstonmethodist.org/, Late Stage, Leadership Team, Jenny Chang, Roberta Schwartz, EVP and Chief Innovation Officer, Recent News, PR Newswire, 2026-08-11, 2026-08-05, American Hospital Association, 2026-07-18, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit, Understand your strength & weakness

Experience

4+ years