Top 44 Clinical study manager Jobs in Houston Tx

Clinical Research Coordinator (CRC)-FT
Evolution Research Group —Houston, TX
- Full-time
- Mid-level
- High school diploma or GED
- Neurology
- Health insurance
- Dental insurance
Quick Apply
Clinical Trial Manager
Immatics US —Houston, TX
- $130,000 - $150,000 a year
- Full-time
- Background check
- Nursing
- Up to 50% travel
- Paid parental leave
- Paid holidays
10d
Study Manager I
DM CLINICAL RESEARCH GROUP —Houston, TX
- $80,000 - $96,000 a year
- Customer service
- 5 years
- Writing skills
Clinical Research Specialist
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Hospital
- Writing skills
- English
Clinical Project Manager
Tranquil Clinical and Research Consulting Services LLC —Friendswood, TX
- Full-time
- Nursing
- Computer Science
- Hospital
Quick Apply
Clinical Research Manager
Tricoastal Narcolepsy and Sleep Disorders Center —Sugar Land, TX
- Weekends as needed
- Background check
- Management
- Patient monitoring
Quick Apply
1d
Clinical Research Specialist - OBGYN
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Hospital
- Writing skills
- English
2d
Clinical Research Coordinator
Pinnacle Clinical Research —Bellaire, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
9d
Clinical Research Coordinator I - Spine
Houston Methodist Academic Institute —Houston, TX
- Full-time
- English
- Mid-level
- Residential
4d
Clinical Trial Research Coordinator I- Imaging
Houston Methodist Academic Institute —Houston, TX
- Full-time
- English
- Mid-level
- Residential
Clinic Manager
DelRicht Research —Jacinto City, TX
- 12 hour shift
- Bachelor of Science
- Mid-level
- 3 years
- Profit sharing
- Disability insurance
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Houston, TX
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Clinical Research Site Manager
Clarius Medical Group, PLLC —Sugar Land, TX
- $65,000 - $72,000 a year
- Full-time
- Mid-level
- 3 years
- Leadership
Quick Apply
Site Manager
DelRicht Research —Houston, TX
- 12 hour shift
- Bachelor of Science
- Mid-level
- 3 years
- Profit sharing
- Disability insurance
Clinical Research Coordinator
Alcanza Clinical Research —Sugar Land, TX
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Associate II - FSP
Precision Medicine Group —Houston, TX
- $91,500 - $137,300 a year
- Online Application
- Remote
- Clean driving record
- Word processing
- Mid-level
Research Program Project Manager - Nanomedicine
Houston Methodist Academic Institute —Houston, TX
- Full-time
- Doctoral degree
- Customer service
- Word processing
Program Manager - Research - Stroke Institute (Dr Savitz)
UTHealth Houston —Houston, TX
- Full-time
- RN License
- 5 years
- University
- Health insurance
- Employee discount
4d
Clinical Research Coordinator II
Helios Clinical Research —Houston, TX
- Full-time
- Vital signs
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Research Coordinator
American Oncology Network, Inc. —Houston, TX
- $49,608.00 - $87,276.80 a year
- Full-time
- Nursing
- RN License
- Customer service
Quick Apply
4d

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Clinical Research Coordinator (CRC)-FT

Evolution Research Group -
Houston, TX

Quick Apply

Job Details

Full-time

Benefits

Health insurance
Dental insurance
Paid time off
401(k) matching

Qualifications

Computer operation
High school diploma or GED
ICH guidelines
Computer skills
Clinical quality assurance standards
FDA regulations

Full Job Description

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Clinical Research Coordinator II is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC II completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities:

General

Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.
Develop draft source documents and review the documents for accuracy and clarity prior to study start up.
Develop a mechanism for subject recruitment and ongoing communications with PCP and nursing staff as appropriate.
Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.
Manage studies with sponsor, and Principal Investigator to ensure compliance with protocol requirements.
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
Communication of all protocol related issues/problems to the appropriate management staff, including but not limited to questions regarding the conduct of the clinical trial.
Contribute to the SOP review and development as delegated by the Site Director.

Study Management

Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.
Attend the investigator meeting for each assigned protocol, as appropriate.
Completion of IRB study renewals and maintain copies of all IRB communications.
In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.
Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator
Review and obtain informed consent from potential study volunteers.
Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations.
Maintain organized, accurate and complete study records including but not limited to regulatory documents, signed informed consents, IRB correspondence/approvals, source documentation, drug dispensing logs, subject logs and study-related communications.
Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.
Ensure timely and accurate CRF completion for each study subject.
In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.
Outcome of enrollment and sponsor monitoring visits of all assigned protocols
Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

Education and experience
- High School Diploma or its equivalent; College degree preferred.
- Two (2) to four (4) years of experience OR certification as a Clinical Research Coordinator
- Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
- Knowledgeable in medical terminology so as to communicate with physician office and laboratory staff.
- Demonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.
- Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
Requirements
- Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
- Excellent communication skills (interpersonal, written, verbal)
- Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

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Refine Your Search

clinical study manager jobs in houston tx

Clinical Research Coordinator (CRC)-FT

Clinical Trial Manager

Study Manager I

Clinical Research Specialist

Clinical Project Manager

Clinical Research Manager

Clinical Research Specialist - OBGYN

Clinical Research Coordinator

Clinical Research Coordinator I - Spine

Clinical Trial Research Coordinator I- Imaging

Clinic Manager

Senior Clinical Research Associate (level dependent on experience)

Clinical Research Site Manager

Site Manager

Clinical Research Coordinator

Clinical Research Associate II - FSP

Research Program Project Manager - Nanomedicine

Program Manager - Research - Stroke Institute (Dr Savitz)

Clinical Research Coordinator II

Clinical Research Coordinator

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