Top 870 Study manager Jobs in Philadelphia Pa

Study Manager I
DM CLINICAL RESEARCH GROUP —Philadelphia, PA
- Customer service
- 5 years
- Writing skills
13d
Manager, Career & Employment Pathways, CCME
Community College of Philadelphia —Philadelphia, PA
- $54,498 - $89,921 a year
- Full-time
- Management
- Research
- 3 years
- Paid holidays
- Disability insurance
Employee Engagement- Associate Business Partner
Philadelphia Gas Works —Philadelphia, PA
- Full-time
- Microsoft Excel
- 5 years
- Employment & labor law
- Free parking
- Health insurance
Work Study Student
Thomas Jefferson University and Hospitals —Philadelphia, PA
- Part-time
- 5 years
- Computer literacy
- Research
- AD&D insurance
- Disability insurance
4h
Research Project Manager
University of Pennsylvania —Philadelphia, PA
- $58,506 - $70,958 a year
- Full-time
- Background check
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Administrative Coordinator
Temple University —Philadelphia, PA
- Full-time
- Hybrid work
- Office
- Analysis skills
- University
- Paid holidays
- Health insurance
Manager of Membership
Pennsylvania Academy of the Fine Arts —Philadelphia, PA
- Full-time
- 3 years
- Analysis skills
- Bachelor's degree
Quick Apply
Part-time Faculty Pool - College of Health Sciences (2026-2027)
Arcadia University —Glenside, PA
- Part-time
- Background check
- Laboratory
- Doctoral degree
- Tuition reimbursement
- Retirement plan
Quick Apply
Part-time Faculty Pool - School of Education (2026-2027)
Arcadia University —Glenside, PA
- Part-time
- Background check
- Doctoral degree
- Mid-level
- Tuition reimbursement
- Retirement plan
Quick Apply
Study Start-Up Manager
CEDENT —Wilmington, DE
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
Integrated Study Timeline Manager
ICON Plc —Blue Bell, PA
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- 5 years
- Disability insurance
- Health insurance
Qualitative Project Manager (Remote)
M3USA —Fort Washington, PA
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
Associate Global Study Coordinator
Suvoda —Philadelphia, PA
- Remote
- Mid-level
- Bachelor's degree
- Data entry
Quick Apply
Clinical Research Project Manager C
University of Pennsylvania —Philadelphia, PA
- $89,500 - $106,940 a year
- Full-time
- Background check
- 5 years
- HIPAA
- Health insurance
- Dental insurance
Vocational Case Manager
Enlyte —Philadelphia, PA
- $72,000 - $85,000 a year
- Full-time
- Hybrid work
- Microsoft Outlook
- Research
- Mid-level
- Travel reimbursement
- Health savings account
Clinical Data Manager
American College of Radiology —Philadelphia, PA
- $73,000 - $80,000 a year
- Online Application
- Remote
- Nursing
- Bachelor's degree
- Senior level
- Tuition reimbursement
- Paid time off
2d
Lecturers, Public Policy & Administration
Rutgers University —Camden, NJ
- From $2,777 a month
- Part-time
- Classroom
- Mid-level
- Master's degree
- Paid holidays
- Dental insurance
Senior Project Manager, Market Research (Remote)
M3USA —Fort Washington, PA
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- 5 years
- Paid holidays
- Disability insurance
Quick Apply
Research Lab Manager
Children’s Hospital of Philadelphia —Philadelphia, PA
- $92,100 - $117,400 a year
- Full-time
- Research
- Analysis skills
- Bachelor's degree
Quick Apply
Clinical Research Coordinator A
University of Pennsylvania —Philadelphia, PA
- $47,313 a year
- Full-time
- Background check
- Management
- Bachelor of Science
- Health insurance
- Dental insurance

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Study Manager I

DM CLINICAL RESEARCH GROUP -
Philadelphia, PA

Apply Now

Job Details

13 days ago

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 philadelphia pa

Study Manager I

Manager, Career & Employment Pathways, CCME

Employee Engagement- Associate Business Partner

Work Study Student

Research Project Manager

Administrative Coordinator

Manager of Membership

Part-time Faculty Pool - College of Health Sciences (2026-2027)

Part-time Faculty Pool - School of Education (2026-2027)

Study Start-Up Manager

Integrated Study Timeline Manager

Qualitative Project Manager (Remote)

Associate Global Study Coordinator

Clinical Research Project Manager C

Vocational Case Manager

Clinical Data Manager

Lecturers, Public Policy & Administration

Senior Project Manager, Market Research (Remote)

Research Lab Manager

Clinical Research Coordinator A

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