Top 797 Study manager Jobs in Scottsdale, Az

Study Manager I
DM CLINICAL RESEARCH GROUP —Phoenix, AZ
- Customer service
- 5 years
- Writing skills
Enrollment Manager - Phoenix Seminary
Phoenix Seminary Inc —Scottsdale, AZ
- Full-time
- Microsoft Outlook
- Sales
- Mid-level
Quick Apply
Senior Global Clinical Study Manager
IQVIA —Phoenix, AZ
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
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
Specialist
National Institute for Excellence in Teaching —Scottsdale, AZ
- Mid-level
- Leadership
Quick Apply
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
Initial Clinical Reviewer - Remote - AZ
Blue Cross Blue Shield of Arizona —Phoenix, AZ
- Full-time
- LMFT
- Nursing
- RN License
Standardized Patient
St Joseph Hospital & Medical Center —Phoenix, AZ
- $23.00 - $32.49 an hour
- PRN
- High school diploma or GED
- Travel
- Neurology
8d
Coordinator
Arizona State University —Tempe, AZ
- $48,600 - $54,000 a year
- Weekends as needed
- Background check
- Mid-level
- Office
- Relocation assistance
9d
Sr Customer Success Manager - Justice
Axon —Scottsdale, AZ
- $86,250 - $138,000 a year
- Email
- Remote
- Bachelor's degree
- US work authorization
- Experience equivalent to degree accepted
- Paid parental leave
- Health insurance
Quick Apply
3d
Sr Category Manager (CPG)
Acosta Group —Scottsdale, AZ
- $85,800 - $100,000 a year
- Full-time
- Hybrid work
- Merchandising
- Mid-level
- Office
Quick Apply
Planner
RVi Planning + Landscape Architecture —Scottsdale, AZ
- Microsoft Excel
- Office
- Analysis skills
- Paid parental leave
- Health savings account
Quick Apply
4d
Staff Project Manager, Robotaxi Operations
Tesla —Phoenix, AZ
- Weekends as needed
- SQL
- Driver's License
- Travel
- Commuter assistance
- Health savings account
11d
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
Professional Services Program Manager
Axon —Scottsdale, AZ
- $87,900 - $140,640 a year
- Email
- Hybrid work
- Google Workspace
- Office
- 3 years
- Paid parental leave
- Health insurance
Quick Apply
Administrative Assistant
Arizona State University —Mesa, AZ
- $22 - $24 an hour
- Part-time
- Background check
- Laboratory
- Mid-level
- Travel reimbursement
- Relocation assistance
Manager, Digital Experience & Optimization
CULTURAL EXPERIENCES ABROAD LLC —Phoenix, AZ
- $100,000 - $110,000 a year
- Full-time
- Marketing
- 5 years
- Office
- Paid parental leave
- Paid holidays
Quick Apply
Clinical Research Coordinator I - Strong Heart Study - Phoenix, Arizona
MedStar Health —Phoenix, AZ
- $49,192 - $87,422 a year
- Full-time
- Surgery
- OSHA
- Inventory management
Project Coordinator, Transition Services, Family and Community Medicine (Northern AZ)
University of Arizona —Phoenix, AZ
- $53,039 - $66,299 a year
- Full-time
- Management
- Experience working with individuals with disabilities
- 5 years
- Paid holidays
- Health insurance
14d

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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 scottsdale, az

Study Manager I

Enrollment Manager - Phoenix Seminary

Senior Global Clinical Study Manager

Job 2970 Program Manager

Customer Success Specialist

Specialist

Customer Advocacy Manager

Initial Clinical Reviewer - Remote - AZ

Standardized Patient

Coordinator

Sr Customer Success Manager - Justice

Sr Category Manager (CPG)

Planner

Staff Project Manager, Robotaxi Operations

Urban Forest Program Manager

Professional Services Program Manager

Administrative Assistant

Manager, Digital Experience & Optimization

Clinical Research Coordinator I - Strong Heart Study - Phoenix, Arizona

Project Coordinator, Transition Services, Family and Community Medicine (Northern AZ)

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