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Experienced Clinical Research Manager
2 months ago
Why Choose Vitalief?
Vitalief is at the forefront of Healthcare consulting, dedicated to enhancing Research and revolutionizing Clinical Trials. We are in search of a skilled and passionate Senior Clinical Research Coordinator to become a vital part of our outstanding team, committed to our mission of making a significant impact on lives through research.
Benefits of Joining Vitalief:
- Contribute meaningfully to our clients' objectives of advancing scientific breakthroughs 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 innovation is encouraged and valued.
- Enjoy a balanced life with 20 PTO (Paid Time Off) 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 healthcare options.
Compensation: Competitive salary based on experience.
Work Environment: This role requires on-site work, with the possibility of remote work after acclimatization.
Key Responsibilities:- Collaborate with clinical research leadership and medical staff to execute protocol-specific tasks such as patient screening, test ordering, specimen collection, and documentation of patient responses for various Oncology trials.
- Act as a key communicator between the organization, investigators, research team members, and sponsors to ensure timely coordination and delivery of services to patients.
- Maintain comprehensive research records for all patients involved in Oncology trials, including consent forms, eligibility documentation, and Case Report Forms (CRF).
- Participate in the preparation for trials, including assessing protocol feasibility, developing preliminary budgets, and preparing regulatory documents.
- Coordinate and conduct trial visits, ensuring patients are informed and procedures are executed according to protocol.
- Evaluate and manage study patients for serious adverse events, ensuring compliance with all regulatory requirements.
- Assist patients in understanding their diagnoses and treatment options, while educating them about relevant clinical research studies.
- A Bachelor's Degree is required.
- At least 2 years of experience as a Clinical Research Coordinator, with a focus on patient recruitment, regulatory compliance, and data management.
- Experience in Oncology clinical research is highly desirable.
- Strong understanding of current Federal Regulations and Good Clinical Practice guidelines.
- Ability to engage compassionately with patients and communicate effectively.
- Proven ability to manage multiple trials simultaneously, demonstrating strong organizational and time management skills.
- Collaborative mindset, capable of working effectively with diverse team members.
- Strong decision-making skills and ability to thrive in a fast-paced environment.
- Proficiency in Microsoft Office is essential.
- Familiarity with EPIC and/or OnCore systems is a plus.
Physical Requirements: The role involves standing, sitting, walking, and lifting up to 20 lbs.
Important Note: Vitalief collaborates with major medical centers and academic institutions, which may require compliance with specific health regulations.
