Top 5287 Study manager Jobs in Texas

Study Manager I
DM CLINICAL RESEARCH GROUP —Houston, TX
- $80,000 - $96,000 a year
- Customer service
- 5 years
- Writing skills
Assessment Manager
Harris County Department of Education —Houston, TX
- $72,514 - $88,975 a year
- Full-time
- Writing skills
- Teaching Certification
- Mid-level
Senior Global Clinical Study Manager
IQVIA —Dallas, TX
- $93,100 - $232,800 a year
- Full-time
- Customer service
- Bachelor's degree
- Continuous improvement
8d
Engagement and Organizing Advisor
Oxfam America —Austin, TX
- $75,000 - $80,000 a year
- Full-time
- Remote
- Spanish
- Writing skills
- Mid-level
Quick Apply
Dir, Learning and Development
PDS Health —Irving, TX
- $153,000 - $207,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Office
- Health insurance
- Dental insurance
2027-2028 Administrative Fellowship
Children's Health —Dallas, TX
- Full-time
- Pediatrics
- Business
- Master of Business Administration
- Paid parental leave
- Health insurance
Clinical Study Project Manager
SGS —Richardson, TX
- Full-time
- Mid-level
- Bachelor's degree
- Business
Quick Apply
Customer Success Manager NOA Higher Ed. Southeast Region (USA Remote)
Turnitin, LLC —Dallas, TX
- $77,700 - $129,500 a year
- Full-time
- Remote
- 5 years
- Senior level
- Communication skills
- Paid holidays
- Health insurance
Quick Apply
Project Manager - Food is Medicine Institute
Tufts University —Texas
- $81,200 - $120,900 a year
- Hybrid work
- Spanish
- Microsoft Excel
- Customer service
Clinical Research Sub-Investigator: PMHNP or PA with CAQ in Psychiatry
Austin Clinical Trial Partners —Austin, TX
- $75 - $85 an hour
- Full-time
- Bilingual
- Background check
- Nursing
- Health insurance
- Dental insurance
Quick Apply
Senior Business Development Manager - Dallas, TX
Triumvirate Environmental —Royse City, TX
- $125,000 - $200,000 a year
- Call employer
- OSHA
- Marketing
- Customer service
- Health insurance
- Dental insurance
9d
PROJECT MANAGER - ENGINEER
Moreno Cardenas Inc. —El Paso, TX
- $65,000 - $105,000 a year
- Full-time
- AutoCAD
- Management
- Engineering
- Health savings account
- Disability insurance
Quick Apply
BIM Manager
Bartlett Cocke General Contractors —Austin, TX
- Up to $120,000 a year
- Full-time
- Microsoft Office
- Bachelor's degree
- Quality control
- Health savings account
- Health insurance
Quick Apply
Radiology Technologist (Radiographer) - Urgent Care - Full Time, Days
Texas Health Resources —Dallas, TX
- 12 hour shift
- BLS Certification
- Urgent Care
- Primary Care
- Paid parental leave
- Health insurance
Development Construction Manager
Ithaca Development, LLC —El Paso, TX
- $75,000 - $90,000 a year
- Full-time
- Background check
- Civil engineering
- Construction site
- Health insurance
- Dental insurance
Quick Apply
Engineer II
QUADVEST LP —Magnolia, TX
- Full-time
- Microsoft Outlook
- Computer literacy
- Bachelor of Science
Museum Operations Manager
The Sixth Floor Museum at Dealey Plaza —Dallas, TX
- $80,000 - $95,000 a year
- Weekends as needed
- CPR Certification
- Ability to walk for extended periods
- Office
- Free parking
- Health savings account
Quick Apply
Manager, Vehicle Services Trainer
Cox Automotive —Dallas, TX
- $89,400 - $134,000 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- No degree
- Paid jury duty
- Paid holidays
Resource Management Director
DHR Health —Edinburg, TX
- Full-time
- Acute care
- Background check
- Spanish
- Continuing education credits
- Health insurance
Quick Apply
Substation Engineer 4
Pedernales Electric Cooperative —Cedar Park, TX
- $115,473.60 - $144,342.00 a year
- Overtime
- Hybrid work
- Computer literacy
- Engineering
- Data analysis skills

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study manager jobs near texas

Study Manager I

DM CLINICAL RESEARCH GROUP -
Houston, TX

Apply Now

Job Details

$80,000 - $96,000 a year

Qualifications

Customer service
Writing skills
High school diploma or GED

Full Job Description

A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. In addition, ensure study enrollment meets or exceed Sponsors' expectations and company goals are achieved on a timely basis.

DUTIES & RESPONSIBILITIES

Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA certifications on a timely basis.
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
Adherence and compliance to the assigned protocols at their respective site(s).
Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to
Sponsor-provided and IRB-approved Protocol Training
All relevant Protocol Amendments Training
Any study-specific Manuals Training as applicable
Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate and timely follow-up on the action items, at their respective site(s).
Make sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study-related documents are utilized and implemented at all times for the assigned protocols at their respective site(s).
Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
Creating and or Reviewing Source Documents for their assigned protocol(s) at their respective site(s) in a timely manner.
Responsible for training the site teams and supporting the adequate conduct of study subject visits, and all other relevant protocol required procedures and documenting these in a timely manner.
Responsible for enforcing ALCOA-C Standards with all the relevant clinical trial documentation.
Responsible for enforcing all Adverse and Serious Adverse Events reporting and any other relevant Safety Information reporting to the appropriate authorities per internal company guidelines, Sponsor, IRB and ICH-GCP Guidelines.
Ensuring data quality, subject retention and compliance, and timely and adequate study data reporting on the assigned protocol(s) being conducted at their respective site(s).
Working with the cross-functional team(s) and site team(s) to ensure study start readiness on all the aspects and adequate training completed by all the relevant site staff prior to FPFV and continue working with the cross-functional team(s) for the successful execution and completion of the clinical trial.
Responsible for clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs and guidance documents.
Working closely with the Associate Site Director/Site Director to achieve strategic goals for the site.
Assist the Associate Site Director/Site Director with staff training and any other relevant tasks assigned.
Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
Strive to ensure weekly, monthly and quarterly assigned goals are met for their respective site(s).
Being prepared for and available at all required company meetings.
Submitting required administrative paperwork per company timelines.
Occasionally attending out-of-town Investigator Meetings.
Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
Facilitate effective communication between patients, healthcare providers, and research staff
Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
Facilitate effective communication between patients, healthcare providers, and research staff
Any other matters as assigned by management.

KNOWLEDGE & EXPERIENCE

Education:

High School Diploma or equivalent required
Bachelor's degree preferred
Foreign Medical Graduates preferred

Experience:

Minimum of 5 years experience in Clinical Research
Supervisory experience preferred
Wide therapeutic range of clinical trials experience preferred
Regulatory research experience is a plus

Credentials:

ACRP or equivalent certification is preferred

Knowledge and Skills:

Goals-driven while continuously maintaining quality.
Must be detailed-oriented, proactive, and able to take initiative.
Must have strong written and communication skills.
Must have excellent customer service skills.
Proficient communication and comprehension skills both verbal and written in the English language are required.
Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred

Apply Now

Refine Your Search

study manager jobs in texas

Study Manager I

Assessment Manager

Senior Global Clinical Study Manager

Engagement and Organizing Advisor

Dir, Learning and Development

2027-2028 Administrative Fellowship

Clinical Study Project Manager

Customer Success Manager NOA Higher Ed. Southeast Region (USA Remote)

Project Manager - Food is Medicine Institute

Clinical Research Sub-Investigator: PMHNP or PA with CAQ in Psychiatry

Senior Business Development Manager - Dallas, TX

PROJECT MANAGER - ENGINEER

BIM Manager

Radiology Technologist (Radiographer) - Urgent Care - Full Time, Days

Development Construction Manager

Engineer II

Museum Operations Manager

Manager, Vehicle Services Trainer

Resource Management Director

Substation Engineer 4

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