Clinical Science Specialist

[Position Summary]

Clinical Science Specialist will play a key role in supporting clinical trial operations and managing investigator-sponsored research (ISR). This role is responsible for clinical research device accountability, research fund management support, employee education, and site management. The position requires strong organizational skills, attention to detail, and the ability to collaborate effectively with internal and external stakeholders. 

[Key Responsibilities]

• Support the planning, coordination, and execution of clinical trials in compliance with regulatory and company requirements

• Manage and oversee Investigator-Sponsored Research (ISR), including initial review, documentation, and ongoing study support

• Ensure proper management of investigational medical devices, including tracking, accountability, and reporting

• Support research fund management processes, including budget tracking and compliance with internal guidelines

• Assist in the development and delivery of training programs for employees on clinical and medical topics

• Coordinate and maintain strong relationships with research institutions, ensuring adherence to protocols and company standards

• Provide administrative and operational support for internal and external audits, inspections, and regulatory submissions

[Required Qualifications]

• Bachelor’s degree in life sciences, nursing, pharmacy, or a related field (advanced degree preferred)

• Previous experience in clinical research, medical affairs, or related functions within the healthcare or medical device industry

• Knowledge of Good Clinical Practice (GCP), relevant regulatory requirements, and clinical trial operations

• Strong communication and organizational skills with the ability to manage multiple tasks simultaneously

• Ability to work independently and collaboratively in a cross-functional team environment

• Proficiency in English (written and spoken) and MS Office applications

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