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Oncology Clinical Research Supervisor
2 months ago
WHY CHOOSE VITALIEF INC.?
Vitalief Inc. is at the forefront of Healthcare consulting, dedicated to enhancing Research and revolutionizing Clinical Trials. We are on the lookout for a skilled and passionate Clinical Research Study Supervisor to become an integral part of our dynamic team. As a full-time employee, you will play a crucial role in our mission to make a significant impact on lives through scientific advancement.
Benefits of Joining Vitalief:
- Be a vital contributor to our clients' efforts in pushing the boundaries of scientific innovation that can positively affect patient outcomes.
- Experience a PEOPLE FIRST culture that emphasizes both personal and professional development for all employees.
- Engage in a collaborative environment where your ideas are valued and innovation is encouraged.
- Enjoy a healthy work-life balance with 20 PTO days and 9 paid holidays each year.
- Benefit from comprehensive offerings including company-paid life insurance, short and long-term disability coverage, a 401K retirement plan, and a variety of robust healthcare options.
Compensation: Competitive salary range of $100,000 to $120,000, commensurate with experience.
Key Responsibilities:
- In collaboration with the Director of Clinical Research Operations, develop and implement workflows and processes that ensure high-quality clinical research for various Oncology trials.
- Ensure compliance with Good Clinical Practice (GCP) guidelines and relevant regulations, while striving to meet the objectives set by the management team.
- Foster effective communication and collaboration with medical staff, executive leadership, and department heads to enhance service delivery and operational efficiency.
- Oversee the daily activities of a clinical research team, providing guidance, support, and training tailored to their needs.
- Exhibit leadership by analyzing staffing requirements and making recommendations for optimal staff utilization.
- Work closely with management to create, implement, and assess standard operating procedures that support the clinical research initiatives.
- Ensure that clinical research activities prioritize patient-centered care.
- Conduct regular Quality Assurance audits with the team to verify data integrity and adherence to research protocols.
- Facilitate the approval of research protocols by the Institutional Review Board and ensure all regulatory documentation is in place prior to protocol initiation.
- Collaborate with physicians, nurses, pharmacy staff, and other stakeholders to ensure timely and coordinated patient services.
- Maintain up-to-date knowledge of relevant guidelines and regulations including DHHS, FDA, OHRP, NIH, GCP, HIPAA, and IRB.
Essential Qualifications:
- Bachelor's Degree in a relevant field such as social sciences.
- A minimum of 5 years of experience in a clinical research setting.
- At least 3 years of experience specifically in Oncology research.
- 1-2 years of supervisory experience in a clinical research context, with experience managing licensed medical professionals being advantageous.
- Strong leadership capabilities and people management skills, with a focus on creating a positive work environment and resolving conflicts effectively.
- Excellent verbal and written communication skills, with the ability to build cross-functional partnerships.
- Strong organizational and time management skills, with a collaborative and adaptable approach.
- Ability to make independent decisions and thrive in a fast-paced environment managing multiple clinical trials.
- Certification from the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (CCRP) is required.
- Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel) and experience with electronic medical records and Clinical Trials Management Systems.
PHYSICAL REQUIREMENTS: Ability to stand, sit, walk, and perform visual tasks. Must be able to lift up to 20 lbs.
IMPORTANT NOTE: Vitalief partners with major medical centers and academic institutions, which may require all on-site personnel to be vaccinated annually for Influenza and pass a Mantoux Tuberculin Skin Test for Mycobacterium Tuberculosis.
