Top 16 Sponsor private investigator Jobs in Florida

Clinical Research Coordinator I
DM CLINICAL RESEARCH GROUP —Bradenton, FL
- Writing skills
- High school diploma or GED
- Bachelor's degree
3d
SPONSORED RESEARCH ADMIN III
Moffitt Cancer Center —Tampa, FL
- Full-time
- Remote
- 6 years
- Analysis skills
- Bachelor's degree
- Health insurance
- Dental insurance
Psychedelic ARNP
Segal Institute for Clinical Research —Lauderhill, FL
- $130,000 - $140,000 a year
- Full-time
- Psychiatry
- Mid-level
- In-person
- Health savings account
- Relocation assistance
Quick Apply
Clinical Research Coordinator
Metabolic Research Institute Inc —West Palm Beach, FL
- $26 - $28 an hour
- Full-time
- Spanish
- Vital signs
- English
- Health insurance
- Dental insurance
Quick Apply
Principal Investigator [Part Time]
Rovia Clinical Research —Miami, FL
- Part-time
- Hybrid work
- Medicine
- 11+ years
- Senior level
Quick Apply
Clinical Research Coordinator-Office of Research
Tallahassee Memorial Healthcare —Tallahassee, FL
- Full-time
- Background check
- Nursing
- Anatomy knowledge
Manager, Grants
New College of Florida —Sarasota, FL
- $65,000 - $70,000 a year
- Full-time
- Master's degree
- University
- Bachelor's degree
Research Regulatory Affairs Specialist I
Florida Cancer Specialists & Research Institute —West Palm Beach, FL
- Full-time
- Background check
- Microsoft Outlook
- Customer service
- Tuition reimbursement
- 401(k) matching
Director of Sponsored Programs
Florida Tech —Melbourne, FL
- Full-time
- Management
- 3 years
- University
1d
Director of Philanthropy, Athletics
Florida Tech —Melbourne, FL
- Full-time
- Marketing
- Master's degree
- University
Assistant Director, Sponsored Programs
University of Central Florida —Orlando, FL
- $89,076 - $111,345 a year
- Full-time
- Office
- Finance
- Master's degree
- Paid holidays
- Health insurance
Director of Philanthropy, College of Psychology & Liberal Arts
Florida Tech —Florida
- Full-time
- Sales
- 5 years
- University
Sr. Manager, Sponsored Programs
University of Miami —Miami, FL
- Full-time
- 5 years
- University
- Bachelor's degree
- Health insurance
- Dental insurance
Executive Director, Research Administration (Pre-Award)
University of Miami —Coral Gables, FL
- Full-time
- Office
- Master's degree
- University
ORA Sr. Manager, Research Administration (Post Award)
University of Miami —Coral Gables, FL
- Full-time
- CPA
- Office
- Master's degree
20h
Assoc. Director, Research Administration_Pre-Award (Special Projects)
University of Miami —Coral Gables, FL
- Full-time
- Hybrid work
- Master's degree
- University
- Bachelor's degree

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Clinical Research Coordinator I

DM CLINICAL RESEARCH GROUP -
Bradenton, FL

Apply Now

Job Details

3 days ago

Qualifications

Writing skills
High school diploma or GED

Full Job Description

The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the 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. The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure 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 Certification on a timely basis.
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.
Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
Submitting required administrative paperwork per company timelines.
Participating in subject recruitment and retention efforts.
Engaging with Research Participants and understanding their concerns.
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 a plus
Foreign Medical Graduates preferred

Experience:

1+ years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
2+ years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting

Credentials:

ACRP or equivalent certification is preferred
Registered Medical Assistant certification or equivalent is preferred

Knowledge and Skills:

Be an energetic, go-getter who is detail-oriented and can multi-task.
Be goals-driven while continuously maintaining quality.
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

sponsor private investigator jobs in florida

Clinical Research Coordinator I

SPONSORED RESEARCH ADMIN III

Psychedelic ARNP

Clinical Research Coordinator

Principal Investigator [Part Time]

Clinical Research Coordinator-Office of Research

Manager, Grants

Research Regulatory Affairs Specialist I

Director of Sponsored Programs

Director of Philanthropy, Athletics

Assistant Director, Sponsored Programs

Director of Philanthropy, College of Psychology & Liberal Arts

Sr. Manager, Sponsored Programs

Executive Director, Research Administration (Pre-Award)

ORA Sr. Manager, Research Administration (Post Award)

Assoc. Director, Research Administration_Pre-Award (Special Projects)

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