Top 30 Investigator Jobs in Waller, Tx

Study Manager II
DM CLINICAL RESEARCH GROUP —Houston, TX
- $80,000 - $96,000 a year
- Customer service
- 5 years
- Writing skills
Division Protective Services Specialist (Houston)
QuikTrip —Houston, TX
- $33.53 - $39.74 an hour
- Background check
- 18 years or older
- CPR Certification
Clinical Research Coordinator
Tara Rizvi, MD —Katy, TX
- Full-time
- HIPAA
- Mid-level
- 3 years
- Health insurance
- 401(k)
Quick Apply
5d
Research Assistant Professor/Research Associate Professor
Prairie View A&M University —Prairie View, TX
- Online Application
- Background check
- 6 years
- Doctoral degree
Clinical Research Coordinator
BRCR Global —Katy, TX
- Full-time
- Spanish
- Customer service
- Mid-level
- Health insurance
- 401(k)
Quick Apply
11d
Unblinded Clinical Research Coordinator II
DM CLINICAL RESEARCH GROUP —Tomball, TX
- Spanish
- Microsoft Outlook
- Customer service
3d
Technical Support and Warranty Investigation specialist
INNIO —Houston, TX
- On call
- 5 years
- ERP systems
- Laboratory experience
Quick Apply
Foster Care Licensed Child Placing Agency Administrator
Circle of Living Hope —Houston, TX
- $50,000 - $75,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Residential
- Paid holidays
- Health insurance
Quick Apply
14d
Clinical Research Coordinator - Onsite
Advanced Rheumatology of Houston —The Woodlands, TX
- $40,000 - $75,000 a year
- Full-time
- Private practice
- Spanish
- Mid-level
- Paid holidays
- Dental insurance
Quick Apply
Postdoctoral Researcher - NRCS
Prairie View A&M University —Prairie View, TX
- Online Application
- Background check
- No experience needed
- Mid-level
Certified Pharmacy Technician
Alcanza Clinical Research —Katy, TX
- Full-time
- Spanish
- HIPAA
- English
- Health savings account
- Disability insurance
Quick Apply
Associate Professor & Executive Director CIRCLE
Prairie View A&M University —Prairie View, TX
- Online Application
- Background check
- Doctoral degree
- University
3d
Director of Clinical Research Operations
Tara Rizvi, MD —Katy, TX
- Full-time
- Bachelor's degree
- Recruiting
- Experience equivalent to degree accepted
- Health insurance
- 401(k)
Quick Apply
5d
Customer Service Representative
Nouryon —Houston, TX
- Full-time
- Microsoft Excel
- Writing skills
- Mid-level
Clinical Research Principal Investigator - Neurologist
Alcanza Clinical Research —Katy, TX
- Part-time
- Spanish
- Medicine
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
Employment Attorney
Spitz, The Employee's Law Firm —Houston, TX
- $65,000 - $90,000 a year
- Writing skills
- Mid-level
- Office
- Gym membership
Quick Apply
Master Electrician - Operations
Trystar Inc —Houston, TX
- Full-time
- Travel
- Senior level
- Communication skills
- Paid holidays
- Disability insurance
Quick Apply
Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island
Vertex Pharmaceuticals —United States
- $171,300 - $256,900 a year
- Full-time
- English
- Mentoring
- Data entry
- Loan repayment program
- Health insurance

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Study Manager II

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

investigator jobs in waller, tx

Study Manager II

Division Protective Services Specialist (Houston)

Clinical Research Coordinator

Research Assistant Professor/Research Associate Professor

Clinical Research Coordinator

Unblinded Clinical Research Coordinator II

Technical Support and Warranty Investigation specialist

Foster Care Licensed Child Placing Agency Administrator

Clinical Research Coordinator - Onsite

Postdoctoral Researcher - NRCS

Certified Pharmacy Technician

Associate Professor & Executive Director CIRCLE

Director of Clinical Research Operations

Customer Service Representative

Clinical Research Principal Investigator - Neurologist

Employment Attorney

Master Electrician - Operations

Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island

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