Site relationship management role ensuring sustainable trial start - up for assigned sites in clinical drug development at Novartis. Collaborating with global teams and ensuring adherence to clinical operations standards and timelines.
About the role
- Clinical Research Specialist advancing neuroscience research at WVU's Rockefeller Neuroscience Institute. Coordinating operational tasks and ensuring compliance in clinical trials focused on brain therapeutics.
Responsibilities
- Facilitate compliance with the requirements of the research protocol and good clinical research practice while remaining cognizant of the needs of diverse populations.
- Utilizes multiple communication methods to facilitate the effective conduct of clinical trials.
- Demonstrates leadership in ensuring patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.
- Involves a variety of resources and strategies to manage the care of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements as well as management of symptoms.
- Provides leadership to the research team in ensuring collection of source data and completion of documentation that validates the integrity of the conduct of the clinical trial.
- Utilizes a variety of strategies to enhance recruitment while being mindful of the needs of a diverse patient population.
- Demonstrates leadership in ensuring adherence to ethical practices during the conduct of clinical trials to protect the rights and well-being of patients and the collection of quality data.
- Identifies the financial variables that affect research and supports good financial stewardship in clinical trials.
Requirements
- Bachelor’s degree from an allied health discipline or related field.
- A minimum of two (2) years of experience in the following: Working in a clinical setting and/or experience working in clinical research.
- Any equivalent combination of related education and/or experience will be considered.
- Knowledge of clinical trials research.
- Effective communication both verbally and in writing.
- Skill in providing customer and personal services.
- Ability to effectively communicate and present information to co-workers, patients and groups.
- Excellent problem-solving skills.
- Within two (2) years of employment, incumbent must obtain certification as a Research Coordinator through the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA).
Benefits
- 37.5-hour work week
- 13 paid holidays
- 24 annual leave (vacation) days per year
- 18 sick days per year
- WVU offers a range of health insurance and other benefits
- 401(a) retirement savings with 6% employee contribution match, eligibility to continue health insurance, and other retiree perks.
- Wellness programs
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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