Wound Care Clinical Trials Principal Investigator - Part Time
Behavioral Health Market Context
Apply Nowvia Aspire Media Group Jobs
Job Description
you will have the responsibility to design, oversee, and execute clinical studies in wound care. You'll work collaboratively with diverse teams, including clinicians, research coordinators, and sponsors, to ensure that our studies adhere to regulatory standards and produce valuable data that contributes to product development and improvements in patient care.
Key Responsibilities:
• Provide direct care to wound care patients through debriding and applying appropriate treatment methods.
• Lead the planning and implementation of wound care clinical trials, from developing study protocols to ensuring successful completion.
• Guarantee compliance with Good Clinical Practice (GCP), Institutional Review Board (IRB), and all relevant regulatory guidelines.
• Oversee data integrity, patient safety, and the ethical conduct of all research activities.
• Engage with internal and external partners, including sponsors, Contract Research Organizations (CROs), and clinical personnel.
• Analyze results and contribute to the creation of publications, presentations, and regulatory submissions.
Qualifications:
• MD, DO, or DPM APP in a relevant field such as wound care, surgery, or dermatology, or professionals with experience in wound care clinical trials.
• In-depth knowledge of wound healing, tissue repair, or related therapeutic areas.
• Strong leadership, communication, and problem-solving abilities.
This position will be based at our clinical centers in Akron, Ohio, and Omaha, Nebraska.
Key Responsibilities:
• Provide direct care to wound care patients through debriding and applying appropriate treatment methods.
• Lead the planning and implementation of wound care clinical trials, from developing study protocols to ensuring successful completion.
• Guarantee compliance with Good Clinical Practice (GCP), Institutional Review Board (IRB), and all relevant regulatory guidelines.
• Oversee data integrity, patient safety, and the ethical conduct of all research activities.
• Engage with internal and external partners, including sponsors, Contract Research Organizations (CROs), and clinical personnel.
• Analyze results and contribute to the creation of publications, presentations, and regulatory submissions.
Qualifications:
• MD, DO, or DPM APP in a relevant field such as wound care, surgery, or dermatology, or professionals with experience in wound care clinical trials.
• In-depth knowledge of wound healing, tissue repair, or related therapeutic areas.
• Strong leadership, communication, and problem-solving abilities.
This position will be based at our clinical centers in Akron, Ohio, and Omaha, Nebraska.
Qualifications
- •MD, DO, or DPM APP in a relevant field such as wound care, surgery, or dermatology, or professionals with experience in wound care clinical trials
- •In-depth knowledge of wound healing, tissue repair, or related therapeutic areas
- •Strong leadership, communication, and problem-solving abilities
Benefits
Responsibilities
- •We're searching for a part-time Principal Investigator to lead groundbreaking clinical trials aimed at improving wound healing, tissue repair, and patient outcomes
- •This is an exciting opportunity for those who want to make a tangible impact in the field of wound care
- •About the Role: As the Principal Investigator, you will have the responsibility to design, oversee, and execute clinical studies in wound care
- •You'll work collaboratively with diverse teams, including clinicians, research coordinators, and sponsors, to ensure that our studies adhere to regulatory standards and produce valuable data that contributes to product development and improvements in patient care
- •Provide direct care to wound care patients through debriding and applying appropriate treatment methods
- •Lead the planning and implementation of wound care clinical trials, from developing study protocols to ensuring successful completion
- •Guarantee compliance with Good Clinical Practice (GCP), Institutional Review Board (IRB), and all relevant regulatory guidelines
- •Oversee data integrity, patient safety, and the ethical conduct of all research activities
- •Engage with internal and external partners, including sponsors, Contract Research Organizations (CROs), and clinical personnel
- •Analyze results and contribute to the creation of publications, presentations, and regulatory submissions
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