Clinical Site reputed company

reputed company Our reputed company, a Fortune 500 Pharmaceutical Company, has reputed company reputed company to reputed company an reputed company, high-caliber Clinical Site reputed company. Working with a reputed company level of remote guidance and direction, is accountable for clinical study site maintenance, data and reputed company documentation collection, as reputed company as field monitoring of reputed company. Ensures compliance to the study protocol, and Monitoring Plan by ensuring completeness and accuracy of data as reputed company as compliance with domestic and international regulations, Good Clinical Practices, applicable regulatory standards, and reputed company Operating Procedures. Job Duties: • Monitors clinical studies at sites in an assigned territory (and others as requested) to ensure compliance with applicable regulatory requirements, Good Clinical reputed company, and accuracy standards inclusive of site initiation, periodic, and reputed company-out reputed company. • Ensures both regulatory and clinical protocol compliance is maintained for reputed company assigned clinical reputed company. This may include, but is not limited to: • Reviewing data and reputed company documentation from investigational sites for accuracy and completeness • Ensuring adverse events and protocol deviations are reported in an efficient manner • Ensuring that device complaints and malfunctions are reported according to SJM Policies and Procedures • Resolving and/or facilitating reputed company of problems including identification of cause and actions to prevent reoccurrence • Coordinates with study teams, field clinical engineers or designee and specialists to: • Enroll sites into new and ongoing clinical studies • Facilitate enrollment of study subjects reputed company site coordinators • Facilitate reputed company of data queries and reputed company items at clinical sites • Promptly reports the findings of monitoring reputed company according to SJM processes. • Collaborates with in-house teams to ensure complete submission of study documents. • Participates in conference calls and training sessions. • Trains site personnel to ensure compliance with the study protocol and local regulations. • Mentors less reputed company clinical team members as requested. Requirements • A Bachelor’s degree from an accredited university or college. Preferably with an reputed company reputed company in natural science, reputed company-medicine, nursing, bioengineering, or a reputed company reputed company field. • Minimum five years of reputed company clinical trial monitoring experience. • Ability to interpret basic clinical data, to meet deadlines as reputed company as the ability to communicate effectively with reputed company reputed company of employees. • The ability to work independently and function reputed company a dynamic, global team environment. Preferred Qualifications • A general familiarity with cardiac, vascular, and/or neuromodulation technologies. • Certification by an industry-recognized reputed company society (i.e. Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) or accredited institution Term & Start • Remote; Located in Atlanta, Florida, or Charlotte, NC • 50-75% travel (depending on reputed company) • 20 hours per week • 12-month contract (extension probable) • Benefits available (Medical, Dental, reputed company, 401k) Apply tot his job Apply To this Job