Clinical Research Associate

Are you a detail-oriented individual with a passion for improving patient outcomes? Do you thrive in a fast-paced, collaborative environment? If so, we have an exciting opportunity for you at Wentworth-Douglass Hospital as a Clinical Research Associate. In this role, you will be responsible for supporting and coordinating clinical research studies to advance medical knowledge and enhance patient care. We are seeking a highly motivated and organized individual with a strong background in healthcare and research methodologies. If you are looking for a challenging and rewarding career in the healthcare industry, we encourage you to apply for this position.

1. Conduct and coordinate clinical research studies: The Clinical Research Associate will be responsible for conducting and coordinating various clinical research studies at Wentworth-Douglass Hospital. This includes developing study protocols, recruiting participants, collecting and analyzing data, and ensuring compliance with regulatory requirements.
2. Ensure patient safety and ethical standards: The successful candidate will be responsible for ensuring that all clinical research studies are conducted in accordance with established ethical and safety standards. This includes obtaining informed consent from participants, monitoring adverse events, and reporting any safety concerns to the appropriate authorities.
3. Collect and analyze data: The Clinical Research Associate will be responsible for collecting, organizing, and analyzing data from various sources, including medical records, surveys, and laboratory tests. They will also be responsible for maintaining accurate and detailed records of all data collected.
4. Collaborate with healthcare professionals: This role requires close collaboration with healthcare professionals, including physicians, nurses, and other researchers. The Clinical Research Associate will work closely with these individuals to ensure that research studies are conducted efficiently and effectively.
5. Maintain regulatory compliance: The successful candidate will be responsible for ensuring that all research studies are conducted in compliance with relevant regulatory requirements, including FDA guidelines, Good Clinical Practice (GCP) standards, and institutional policies.
6. Communicate study progress: The Clinical Research Associate will be responsible for providing regular updates on study progress to the research team, as well as to external stakeholders, such as study sponsors and regulatory bodies.
7. Develop and maintain study documents: This role requires the development and maintenance of various study documents, including protocols, case report forms, and study manuals. The Clinical Research Associate will be responsible for ensuring that these documents are accurate, complete, and up-to-date.
8. Adhere to study timelines and budgets: The successful candidate will be responsible for managing study timelines and budgets to ensure that all research activities are completed on time and within budget.
9. Contribute to study design and methodology: The Clinical Research Associate will be responsible for

According to JobzMall, the average salary range for a Clinical Research Associate in Boston, MA, USA is between $60,000 and $110,000 per year. However, the actual salary may vary depending on factors such as education, experience, and employer. Additionally, this range may also vary based on the specific job responsibilities and duties of the Clinical Research Associate.

Wentworth-Douglass Hospital is the Seacoast's leading not-for-profit medical center with comprehensive services including walk-in care & physician practices. Hospital includes 178-bed Magnet® Recognized hospital, several urgent care and walk-in care facilities, multiple testing centers, 36 Wentworth Health Partners primary care and specialty care provider practices, The Works Health and Fitness Center and the Wentworth-Douglass Foundation.