Top 65 Clinical study manager Jobs in Philadelphia Pa

Study Manager I
DM CLINICAL RESEARCH GROUP —Philadelphia, PA
- Customer service
- 5 years
- Writing skills
12d
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
23h
Clinical Research Coordinator/Data Manager
Thomas Jefferson University and Hospitals —Philadelphia, PA
- Full-time
- Mid-level
- Master's degree
- High school diploma or GED
- AD&D insurance
- Disability insurance
7d
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
Clinical Research Project Manager
Thomas Jefferson University and Hospitals —Philadelphia, PA
- Full-time
- 3 years
- Master's degree
- University
- AD&D insurance
- Disability insurance
Clinical Research Program Manager
University of Pennsylvania —Philadelphia, PA
- $75,804 - $81,441 a year
- Full-time
- Microsoft Word
- Background check
- Blood sampling
- Health insurance
- Dental insurance
Clinical Research Coordinator
Flourish Research —Philadelphia, PA
- $25 - $36 a year
- Full-time
- Vital signs
- HIPAA
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Project Manager B
University of Pennsylvania —Philadelphia, PA
- $74,500 - $95,000 a year
- Full-time
- Background check
- 5 years
- Writing skills
- Health insurance
- Dental insurance
Clinical Research Associate II/III - US
Optimapharm d.o.o. —Philadelphia, PA
- $75,000 - $100,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Mid-level
- Health insurance
- Dental insurance
Clinical Research Project Manager B (Department of Obstetrics and Gynecology)
University of Pennsylvania —Philadelphia, PA
- $75,804 - $89,789 a year
- Full-time
- Background check
- 5 years
- Master's degree
- Health insurance
- Dental insurance
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Philadelphia, PA
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Health insurance
- Dental insurance
Clinical Trial Manager
Impulse Dynamics —Marlton, NJ
- $95,000 - $115,000 a year
- Bachelor's degree
- Organizational skills
- Senior level
- Paid holidays
- Health insurance
Quick Apply
Clinical Trial Manager
Avalo Therapeutics —Chesterbrook, PA
- Hybrid work
- 5 years
- Office
- Bachelor's degree
Quick Apply
Associate Global Study Coordinator
Suvoda —Philadelphia, PA
- Remote
- Mid-level
- Bachelor's degree
- Data entry
Quick Apply
Research Program Manager
University of Pennsylvania —Philadelphia, PA
- $57,500 - $65,000 a year
- Full-time
- Background check
- Mid-level
- University
- Health insurance
- Dental insurance
Study Start-Up Manager
CEDENT —Wilmington, DE
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
Research Project Manager A
University of Pennsylvania —Philadelphia, PA
- $63,085 - $70,958 a year
- Full-time
- Background check
- Mid-level
- Windows
- Health insurance
- Dental insurance
Clinical Trial Manager
KPS Life —Malvern, PA
- Nursing
- Anatomy knowledge
- 5 years
4d
Senior Clinical Project Manager
ICON Plc —Blue Bell, PA
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Travel
- Disability insurance
- Health insurance
Clinical Research Coordinator II
Cooper University Hospital —Camden, NJ
- $29 - $48 an hour
- Full-time
- Microsoft Outlook
- Mid-level
- 3 years
- Health insurance
- Dental insurance

I want to receive the latest job alert for clinical study manager in philadelphia pa

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical study manager jobs near philadelphia pa

Senior Clinical Research Associate jobs in Philadelphia, PA

Program Manager jobs in Philadelphia, PA

Clinical Research Manager jobs in Philadelphia, PA

Clinical Research Associate jobs in Philadelphia, PA

Clinical Program Manager jobs in Philadelphia, PA

Clinical Data Manager jobs in Philadelphia, PA

Clinical Research Coordinator jobs in Philadelphia, PA

Study Manager jobs in Philadelphia, PA

Research Project Manager jobs in Philadelphia, PA

Senior Clinical Research Associate jobs in Minneapolis, MN

Greenspring Village By Erickson Senior Living jobs in Springfield, VA

Senior Clinical Research Associate jobs in Atlanta, GA

Clinical Research Coordinator jobs in Grand Rapids, MI

Senior Pastor jobs in Tennessee

Senior Clinical Research Associate jobs in Nashua, NH

Wealth Management Client Service Associate jobs in Seattle, WA

Senior Clinical Research Associate jobs in Pittsburgh, PA

Program Manager jobs in Maine

Program Manager jobs in Santa Clarita, CA

Onsite Property Manager jobs in California

Study Manager I

DM CLINICAL RESEARCH GROUP -
Philadelphia, PA

Apply Now

Job Details

12 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

clinical study manager jobs in philadelphia pa

Study Manager I

Clinical Data Manager

Clinical Research Coordinator/Data Manager

Clinical Research Project Manager C

Clinical Research Project Manager

Clinical Research Program Manager

Clinical Research Coordinator

Clinical Research Project Manager B

Clinical Research Associate II/III - US

Clinical Research Project Manager B (Department of Obstetrics and Gynecology)

Senior Clinical Research Associate - US

Clinical Trial Manager

Clinical Trial Manager

Associate Global Study Coordinator

Research Program Manager

Study Start-Up Manager

Research Project Manager A

Clinical Trial Manager

Senior Clinical Project Manager

Clinical Research Coordinator II

I want to receive the latest job alert for clinical study manager in philadelphia pa

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected