D&H National Research Center is hiring: Oncologist for Clinical Research in Margate
Behavioral Health Market Context
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Job Description
in a clinical trial company is not required as we provide training for candidates without prior experience.
This role also offers the potential for great part-time residual income.
Key Responsibilities:
- Protect the rights, safety, and welfare of participants under your care.
- Ensure that clinical trials are conducted according to the investigational plan and all applicable regulations.
- Administer test articles to subjects or delegate this responsibility to nursing staff where appropriate.
- Review and evaluate protocols while providing clinical and scientific support.
- Interact with regulatory bodies relevant to clinical operations.
- Attend study initiation meetings.
- Present protocols at IRB/IEC meetings, as required.
- Assist Operations and Client Managers during sponsor visits.
- Conduct pre-study physical examinations and review lab data to ensure that volunteers meet all inclusion/exclusion criteria.
- Perform on-study and post-study physical examinations to ensure the physical and mental well-being of volunteers.
- Review and sign case report forms (CRFs) at the conclusion of the study.
- Delegate responsibilities as appropriate.
- Act as Principal Investigator or Co-Investigator.
Education/Qualifications:
- MD or DO degree.
- Active and unrestricted Florida Medical License and DEA registration.
Experience:
- Ability to travel to our clinics in Miami to Margate, Florida.
- Strong interpersonal and communication skills.
Job Types: Contract, Part-time
Supplemental Pay:
- Signing bonus
Ability to Commute/Relocate:
- Candidates must be able to reliably commute between sites in Miami, FL 33155 to Margate, FL 33063 .
Education:
- Doctorate (Required)
License/Certification:
- Medical License in the United States (Florida Required)
Willingness to Travel:
- 25% (Preferred)
Work
Location: In-person
This role also offers the potential for great part-time residual income.
Key Responsibilities:
- Protect the rights, safety, and welfare of participants under your care.
- Ensure that clinical trials are conducted according to the investigational plan and all applicable regulations.
- Administer test articles to subjects or delegate this responsibility to nursing staff where appropriate.
- Review and evaluate protocols while providing clinical and scientific support.
- Interact with regulatory bodies relevant to clinical operations.
- Attend study initiation meetings.
- Present protocols at IRB/IEC meetings, as required.
- Assist Operations and Client Managers during sponsor visits.
- Conduct pre-study physical examinations and review lab data to ensure that volunteers meet all inclusion/exclusion criteria.
- Perform on-study and post-study physical examinations to ensure the physical and mental well-being of volunteers.
- Review and sign case report forms (CRFs) at the conclusion of the study.
- Delegate responsibilities as appropriate.
- Act as Principal Investigator or Co-Investigator.
Education/Qualifications:
- MD or DO degree.
- Active and unrestricted Florida Medical License and DEA registration.
Experience:
- Ability to travel to our clinics in Miami to Margate, Florida.
- Strong interpersonal and communication skills.
Job Types: Contract, Part-time
Supplemental Pay:
- Signing bonus
Ability to Commute/Relocate:
- Candidates must be able to reliably commute between sites in Miami, FL 33155 to Margate, FL 33063 .
Education:
- Doctorate (Required)
License/Certification:
- Medical License in the United States (Florida Required)
Willingness to Travel:
- 25% (Preferred)
Work
Location: In-person
Qualifications
- •MD or DO degree
- •Active and unrestricted Florida Medical License and DEA registration
- •Ability to travel to our clinics in Miami to Margate, Florida
- •Strong interpersonal and communication skills
- •Candidates must be able to reliably commute between sites in Miami, FL 33155 to Margate, FL 33063
- •Doctorate (Required)
- •Medical License in the United States (Florida Required)
- •Willingness to Travel:
Benefits
- •Salary: 104,440.00 - $340,987.00
- •This role also offers the potential for great part-time residual income
- •Supplemental Pay:
- •Signing bonus
Responsibilities
- •Protect the rights, safety, and welfare of participants under your care
- •Ensure that clinical trials are conducted according to the investigational plan and all applicable regulations
- •Administer test articles to subjects or delegate this responsibility to nursing staff where appropriate
- •Review and evaluate protocols while providing clinical and scientific support
- •Interact with regulatory bodies relevant to clinical operations
- •Attend study initiation meetings
- •Present protocols at IRB/IEC meetings, as required
- •Assist Operations and Client Managers during sponsor visits
- •Conduct pre-study physical examinations and review lab data to ensure that volunteers meet all inclusion/exclusion criteria
- •Perform on-study and post-study physical examinations to ensure the physical and mental well-being of volunteers
- •Review and sign case report forms (CRFs) at the conclusion of the study
- •Delegate responsibilities as appropriate
- •Act as Principal Investigator or Co-Investigator
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