RN - Clinical Research Coordinator - Oncology - Hematologic Malignancies
South Portland, MEFull-time
80K–110K a year
Behavioral Health Market Context
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Job Description
rials for patients with blood cancers, contributing to the development of new and innovative treatments. As an essential member of our research team, you will bring your nursing expertise, attention to detail, and passion for improving patient outcomes to the forefront of cutting-edge cancer research. If you possess a strong background in oncology nursing and a desire to make a positive impact on the lives of those affected by hematologic malignancies, we encourage you to apply for this exciting opportunity.
Coordinate and oversee all aspects of clinical trials for patients with hematologic malignancies, including patient recruitment, consent, and follow-up care.
Collaborate with physicians and other healthcare professionals to ensure accurate and timely implementation of clinical trial protocols.
Manage and maintain accurate and up-to-date documentation of clinical trial data, including patient records, lab results, and adverse events.
Ensure compliance with all regulatory guidelines and protocols for conducting clinical trials, including obtaining necessary approvals and reporting requirements.
Serve as a liaison between patients, healthcare providers, and research sponsors to facilitate open communication and adherence to study protocols.
Provide education and support to patients and their families regarding the clinical trial process, including potential risks and benefits.
Monitor patient responses and report any adverse events or changes in condition to the research team and regulatory bodies as required.
Collaborate with the research team to analyze and interpret data from clinical trials and assist in the preparation of research publications.
Participate in ongoing training and professional development opportunities to stay current on advancements in oncology and clinical research.
Maintain a high level of professionalism and ethical standards in all interactions with patients, colleagues, and research sponsors.
Mainehealth is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Coordinate and oversee all aspects of clinical trials for patients with hematologic malignancies, including patient recruitment, consent, and follow-up care.
Collaborate with physicians and other healthcare professionals to ensure accurate and timely implementation of clinical trial protocols.
Manage and maintain accurate and up-to-date documentation of clinical trial data, including patient records, lab results, and adverse events.
Ensure compliance with all regulatory guidelines and protocols for conducting clinical trials, including obtaining necessary approvals and reporting requirements.
Serve as a liaison between patients, healthcare providers, and research sponsors to facilitate open communication and adherence to study protocols.
Provide education and support to patients and their families regarding the clinical trial process, including potential risks and benefits.
Monitor patient responses and report any adverse events or changes in condition to the research team and regulatory bodies as required.
Collaborate with the research team to analyze and interpret data from clinical trials and assist in the preparation of research publications.
Participate in ongoing training and professional development opportunities to stay current on advancements in oncology and clinical research.
Maintain a high level of professionalism and ethical standards in all interactions with patients, colleagues, and research sponsors.
Mainehealth is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Qualifications
Benefits
Responsibilities
- •In this role, you will play a critical role in conducting and coordinating clinical trials for patients with blood cancers, contributing to the development of new and innovative treatments
- •As an essential member of our research team, you will bring your nursing expertise, attention to detail, and passion for improving patient outcomes to the forefront of cutting-edge cancer research
- •Coordinate and oversee all aspects of clinical trials for patients with hematologic malignancies, including patient recruitment, consent, and follow-up care
- •Collaborate with physicians and other healthcare professionals to ensure accurate and timely implementation of clinical trial protocols
- •Manage and maintain accurate and up-to-date documentation of clinical trial data, including patient records, lab results, and adverse events
- •Ensure compliance with all regulatory guidelines and protocols for conducting clinical trials, including obtaining necessary approvals and reporting requirements
- •Serve as a liaison between patients, healthcare providers, and research sponsors to facilitate open communication and adherence to study protocols
- •Provide education and support to patients and their families regarding the clinical trial process, including potential risks and benefits
- •Monitor patient responses and report any adverse events or changes in condition to the research team and regulatory bodies as required
- •Collaborate with the research team to analyze and interpret data from clinical trials and assist in the preparation of research publications
- •Participate in ongoing training and professional development opportunities to stay current on advancements in oncology and clinical research
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