The Clinical Trial Associate (CTA) plays a key role in supporting Glooko's Clinical Research projects. This role will be a good fit for candidates who desire to learn and grow professionally while gaining experience in Clinical Trial management. The CTA will assist with existing clinical projects and management of accounts/clinical studies, using knowledge of Glooko products and managing individual projects. This includes managing clinical/outcomes research projects to ensure Clinical Research opportunities are executed and set up for success.
Areas of Responsibility:
- Responsible for supporting external, internal, decentralized, and virtual Clinical Trials and registries.
- Supporting operational aspects of Clinical Trials, including the development of study and source materials (SOPs, IRB forms, etc.).
- Supporting internal departmental quality compliance.
- Contribute to the development, implementation, execution, and follow-up of clinical research and development activities to meet business goals and objectives.
Core Responsibilities:
- Coordinate multiple ongoing clinical research studies.
- Responsible for ordering and tracking of study supplies and device provisioning for multiple clinical studies.
- Work closely with the Customer Support and Product/Engineering teams to track reported issues to ensure follow-up and regular communication with the study sponsor/site staff.
- Work closely with the Data Science team to ensure the quality of Clinical Trials and data analysis.
- Assist with the development and maintenance of training materials in collaboration with Customer Support and Marketing.
- Ensure compliance with SOPs and regulatory requirements (e.g., GCP and US and OUS guidelines).
- Participate in project and departmental team meetings.
- Track and record safety concerns and adverse events/SAEs.
- Participate in product improvement activities (information gathering, requirements, cross-functional meetings) that meet our customers' needs.
- Understand diabetes and comorbid conditions.
- Special projects as assigned
Qualifications and Requirements:
- Excited to work on a team that cares deeply about helping those living with chronic conditions.
- Bachelor's degree or equivalent in a related field with 1-2 years of experience in Clinical Trials.
- Knowledge of digital health solutions and applications preferred.
- Knowledge of the clinical research process preferred.
- Excellent organization and customer service skills.
- Possess problem-solving skills, attention to detail, and resourcefulness; respect and responsibility are critical to success in this role.
- Able to work independently to manage clinical tasks and deliverables to meet timelines with a customer service orientation.
- Strong interpersonal and communication skills across all levels of the organization.
- Ability to collaborate cross-functionally with internal and external key stakeholders including the clinical studies team, data management, clinical site investigators, global clinical, and other internal customers.
- Commitment to individual and team success.
- Is responsive and approaches work with a bias for action. Will thrive in a fast-paced, changing environment with limited structure that requires flexibility, resourcefulness, efficiency, and communicate effectively in a remote environment.
- Travel for customer meetings and conferences may be required for up to 10%.
About Glooko:
There are over 420 million people in the world with diabetes and Glooko helps them, as well as their physicians and care team, manage the disease more easily and cost effectively. Glooko is the Unified Platform for Diabetes Management and provides an FDA cleared, HIPAA compliant Web and Mobile (iOS and Android) application for people with diabetes and the clinicians who treat them. The platform seamlessly unifies data from over 80 of the leading blood glucose meters, insulin pumps, continuous glucose monitors, activity trackers, and biometric devices to deliver insights that improve personal and clinical decision support.
Glooko's mobile app and web dashboard enable patients to easily track and proactively manage all aspects of their diabetes care. Glooko's Population Tracker and APIs offer diabetes-centric analytics and supply insightful reports, graphs and pattern-triggered notifications to patients, health systems, and payers. The Glooko platform also allows customers and third-party developers to create branded modules for Glooko users.
Launched in 2010, Glooko is funded and managed by visionary technologists and leaders in healthcare.
Glooko Benefits Include:
- Having a meaningful impact on people's lives
- Competitive salary based on experience
- Pre-IPO stock incentives
- Full benefits: medical, dental, vision, and transportation incentives
- Annual reimbursement on fitness expenses (gym memberships, running shoes, yoga classes, etc.)
- 401(k) matching program
- Have a meaningful impact on people's lives
Glooko provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, or disability. In addition to federal law requirements, Glooko complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Posted positions are not open to third party recruiters/agencies and unsolicited resume submissions will be considered free referrals.