Clinical Research Coordinator (CRC) Jobs

JJRT, located in Raynham, MA is looking for a Sr. Clinical Data Coordinator (clinical data). This person will be responsible for overall database maintenance, data quality, and project management. Interacts with clinical team on a daily basis to ensure overall quality and integrity of the data. Mentor junior staff/contractors in the data editing and validation process. Develop Case Report Forms. Conduct and oversee Data Review and Validation procedures (data review; query integration). Responsible for the building and management of Oracle Clinical databases, and supporting documentation, such as CRF completion guidelines, data entry guidelines, CRF annotations, and edit check specifications. Identify and resolve issues related to electronically loaded data and clinical data. Responsible for assisting with the creation and programming of validation procedures. Oversee coding process of adverse events and medications/treatments. Assure accurate DCF content and updates of resolutions from sites. Review data reports and listings for appropriate handling and outliers or potential trends of clinical importance. Participate in project planning, preliminary study set up meeting, and vendor selection that involves identifying data management components that need to be considered for inclusion in the protocol, database build, project scoping, and vendor contracts (types of electronic data, clinical assessments, translations, review of research literature for possible study design and database build elements that could impact decisions around study set-up and management). Participate in interviewing candidates. Contribute to the selection process/recruiting qualified staff. Coach new and present staff to remain committed to building a stronger business unit. Provide support and recommendations for improving operations and training of existing and new staff. Define and manage guidelines around data management processes. Interact and collaborate with internal and external customers. Adhere to SEP and GCP processes and procedures.

A minimum of a Bachelors degree n related field (i.e. Life Sciences with an interest in Statistics, Computer Science or Mathematics) or equivalent pharmaceutical industry experience. A minimum of 5 years of clinical data management experience (i.e. Clinical Data Manager role). Computer skills including experience with data entry and database management systems. Good analytical and problem solving skills with attention to detail. Knowledge of clinical trials and clinical trial administration. Excellent oral and written communication skills. Committed to meeting timelines and maintaining a high standard of quality. Self-motivated and able to advance own knowledge in clinical trials data management. Previous work with a CRO in a data management role highly valued. Also highly valued is experience with ACCESS, Oracle Clinical, SAS and SQL. 5% travel is required.

If you want to explore the many small-company environments behind the big-company impact of the Johnson && Johnson Family of Companies, bid on this position today!

For moe information please visit: http://www.jnj.com