Top 1237 Study manager Jobs in Arizona

Study Manager I
DM CLINICAL RESEARCH GROUP —Phoenix, AZ
- Customer service
- 5 years
- Writing skills
Senior Global Clinical Study Manager
IQVIA —Gilbert, AZ
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Enrollment Manager - Phoenix Seminary
Phoenix Seminary Inc —Scottsdale, AZ
- Full-time
- Microsoft Outlook
- Sales
- Mid-level
Quick Apply
Job 2970 Program Manager
State of Arizona —Phoenix, AZ
- $81,000 - $94,000 a year
- Full-time
- Remote
- Public speaking
- 3 years
- Bachelor's degree
- Paid holidays
- Disability insurance
Customer Success Specialist
1Valet —Phoenix, AZ
- $60,000 a year
- Full-time
- Remote
- Computer Science
- Marketing
- Mid-level
- Paid holidays
- Work from home
Quick Apply
Urban Forest Program Manager
City of Mesa, AZ —Mesa, AZ
- $88,949.33 - $124,603.65 a year
- Full-time
- Spanish
- Research
- 3 years
7d
Customer Advocacy Manager
Thales —Chandler, AZ
- $89,747 - $161,183 a year
- Full-time
- Remote
- Background check
- Marketing
- 5 years
- Health savings account
- AD&D insurance
Compliance Coordinator
MT. GRAHAM REGIONAL MEDICAL CENTER INC. —Safford, AZ
- 18 years or older
- Hospital
- English
Quick Apply
Senior Project Manager (Land Development) - Phoenix
RICK ENGINEERING COMPANY —Phoenix, AZ
- $145,000 - $160,000 a year
- Full-time
- Residential
- Bachelor's degree
- Mentoring
- Profit sharing
- Disability insurance
Quick Apply
EH&S Manager
Amcor —Tolleson, AZ
- Full-time
- Bachelor of Science
- Bachelor's degree
- Conflict management
- Paid parental leave
- Health savings account
Quick Apply
Automotive Sales Professional
RIGHT HONDA —Scottsdale, AZ
- $80,000 - $200,000 a year
- Full-time
- Background check
- Sales
- Dealership
- Health insurance
- Dental insurance
Quick Apply
Corporate Safety Director
KEAR Civl Corporation —Phoenix, AZ
- $105,365.00 - $183,713.99 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- OSHA
- Health savings account
- Relocation assistance
Quick Apply
FIRE CHIEF
Town Management —Superior, AZ
- $88,244 - $93,539 a year
- Full-time
- Background check
- Residential
- Driver's License
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I - Nurse
Iterative Health —Tucson, AZ
- Nursing
- RN License
- Quality control
Quick Apply
Commercial Real Estate Transaction Coordinator
Keyser Commercial Real Estate —Scottsdale, AZ
- $55,000 - $70,000 a year
- Full-time
- Microsoft Outlook
- Research
- Mid-level
- Health savings account
- Health insurance
Quick Apply
4d
RN Clinical Research - PRN
Professional Case Management —Page, AZ
- $60 an hour
- PRN
- CPR Certification
- Nursing
- Clean driving record
- On-the-job training
Quick Apply
LPN (Day Shift 6a-6p) *Must have Skills for a High Acuity Unit - Palm Valley Post Acute
Palm Valley Post Acute —Goodyear, AZ
- Full-time
- CPR Certification
- Nursing
- Experience working with individuals with disabilities
Quick Apply
5d
Principal Mechanical Engineer
Raytheon —Tucson, AZ
- $107,500 - $204,500 a year
- Full-time
- Travel
- Mentoring
- In-person
- Paid holidays
- Disability insurance
Senior Development Manager
Lars Andersen & Associates, Inc. —Phoenix, AZ
- Full-time
- Civil engineering
- 7 years
- Construction site
- Health insurance
- Dental insurance
Quick Apply
4d
Sr Principal Electrical Subsystem Architect
Raytheon —Tucson, AZ
- $132,400 - $251,600 a year
- Full-time
- 7 years
- Master's degree
- Doctor of Philosophy
- Paid holidays
- Disability insurance

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Study Manager I

DM CLINICAL RESEARCH GROUP -
Phoenix, AZ

Apply Now

Job Details

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 arizona

Study Manager I

Senior Global Clinical Study Manager

Enrollment Manager - Phoenix Seminary

Job 2970 Program Manager

Customer Success Specialist

Urban Forest Program Manager

Customer Advocacy Manager

Compliance Coordinator

Senior Project Manager (Land Development) - Phoenix

EH&S Manager

Automotive Sales Professional

Corporate Safety Director

FIRE CHIEF

Clinical Research Coordinator I - Nurse

Commercial Real Estate Transaction Coordinator

RN Clinical Research - PRN

LPN (Day Shift 6a-6p) *Must have Skills for a High Acuity Unit - Palm Valley Post Acute

Principal Mechanical Engineer

Senior Development Manager

Sr Principal Electrical Subsystem Architect

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

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