Top 5125 Study manager Jobs in Texas

Study Manager I
DM CLINICAL RESEARCH GROUP —Sugar Land, TX
- Customer service
- 5 years
- Writing skills
Clinical Study Manager
Argon Medical Devices Inc —Plano, TX
- Full-time
- 3 years
- Master's degree
- Continuous improvement
Clinical Study Project Manager
SGS —Richardson, TX
- Full-time
- Mid-level
- Bachelor's degree
- Business
Quick Apply
Study Start-Up (SSU) Manager
DM CLINICAL RESEARCH GROUP —Houston, TX
- Google Workspace
- Management
- 3 years
17h
Senior Global Clinical Study Manager
IQVIA —Dallas, TX
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Healthcare Compliance Investigations Manager
NorthStar Anesthesia —Irving, TX
- Full-time
- Microsoft Excel
- HIPAA
- Analysis skills
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
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
Governance Specialist
Texas Municipal League Intergovernmental Risk Pool —Austin, TX
- Full-time
- Clean driving record
- Microsoft Outlook
- Computer literacy
- Health savings account
- Health insurance
1d
Sub l /Nurse Practitioner
Evolution Research Group —San Antonio, TX
- $100,000 - $150,000 a year
- Full-time
- Presentation skills
- Team management
- Neurology
- Health insurance
- Dental insurance
Quick Apply
Physician (Gastroenterologist) - EDRP Eligible
US Veterans Health Administration —Temple, TX
- $370,000 - $400,000 a year
- Weekends as needed
- Background check
- Medicine
- Management
- Paid holidays
- Loan repayment program
Grain Merchandiser
White Energy —Houston, TX
- Full-time
- Merchandising
- Mid-level
- Office
- Health savings account
- Paid holidays
Quick Apply
Quality Assurance Procedures Administrator
Waste Control Specialist LLC —Andrews, TX
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Dental insurance
Quick Apply
Clinical Trials Nurse Manager
The Center for Cancer and Blood Disorders —Fort Worth, TX
- Full-time
- Nursing
- LVN
- RN License
- Health insurance
- Dental insurance
Quick Apply
Regional Compliance Manager
Zollege —Austin, TX
- $65,000 - $85,000 a year
- Full-time
- Hybrid work
- Google Workspace
- 5 years
- Writing skills
- Travel reimbursement
Quick Apply
7d
Distribution Systems Design Engineer
Moreno Cardenas Inc. —El Paso, TX
- $55,000 - $75,000 a year
- Full-time
- Computer literacy
- System design
- Mid-level
- Health insurance
- Paid time off
Quick Apply
12d
Mechanical Engineer
Precinmac —Lewisville, TX
- Full-time
- Research
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
Outside Sales Representative - Climate Control
Sunbelt Rentals, Inc. —Carrollton, TX
- $40,000 - $62,965 a year
- Full-time
- Mid-level
- Driver's License
- Project management
- Disability insurance
- Health insurance
Quick Apply
Professional Construction Estimator
Rucoba & Maya Construction, LLC —Kyle, TX
- $85,000 - $120,000 a year
- Full-time
- Mid-level
- Office
- 3 years
- Health insurance
- Cell phone reimbursement
Quick Apply
20h
Water Resources Engineer III - Ecological Restoration
Resource Environmental Solutions LLC —Austin, TX
- Remote
- Construction site
- 5 years
- Quality control

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study manager jobs near texas

Study Manager I

DM CLINICAL RESEARCH GROUP -
Sugar Land, TX

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Job Details

Qualifications

Customer service
Writing skills
High school diploma or GED

Full Job Description

A Study Manager I 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

Clinical Study Manager

Clinical Study Project Manager

Study Start-Up (SSU) Manager

Senior Global Clinical Study Manager

Healthcare Compliance Investigations Manager

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

PROJECT MANAGER - ENGINEER

Governance Specialist

Sub l /Nurse Practitioner

Physician (Gastroenterologist) - EDRP Eligible

Grain Merchandiser

Quality Assurance Procedures Administrator

Clinical Trials Nurse Manager

Regional Compliance Manager

Distribution Systems Design Engineer

Mechanical Engineer

Outside Sales Representative - Climate Control

Professional Construction Estimator

Water Resources Engineer III - Ecological Restoration

I want to receive the latest job alert for study manager in texas

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