Medtronic Clinical Studies Support Coordinator IV - Surgical Robotics (Open to Remote) in North Haven, Connecticut
Clinical Studies Support Coordinator IV - Surgical Robotics (Open to Remote)
North Haven, Connecticut, United States
6 days ago
Careers That Change Lives:
The Clinical Studies Support Coordinator IV in the Surgical Robotics Operating Unit supports clinical studies by executing and maintaining one or more of the following areas: document management, data coordination/management, and site management. Serves as liaison between clinical, site, and field personnel, as appropriate, by coordinating and contributing to ongoing, timely and consistent communication. Maintains general knowledge and application of industry practices, regulations, and standards. General application of clinical trial management concepts and principles.
We believe that when people from different cultures, genders, and points of view come together, innovation is the result and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive. To learn more about Inclusion Diversity at MedtronicClick Here (https://www.medtronic.com/us-en/about/careers/diversity-inclusion.html)
Surgical Robotics employees believe that every patient around the world deserves access to quality care and improved outcomes. Driven by our Mission, we believe that surgical robotics can add value to the healthcare ecosystem, lessen variability, and help more people around the world get better, faster.
Were making that exciting future possible and disrupting one of the biggest and fastest growing markets in healthcare with a game-changing portfolio of robotic and data analytics technologies, services, and solutions.
Location: North Haven, Connecticut or Remote
A Day in the Life
Responsibilities may be included the following and other duties may be assigned. Supports clinical studies by executing and maintaining one or more of the following areas with limited supervision.
Provide project/program coordination and support to Global Clinical Study team
Maintains study-specific correspondence and other required documentation
Assists/coordinates in the organization and distribution of clinical study documentation
May assist in tracking study activity, such as start-up progress by ensuring receipt of proper study documentation, agreements, and site approvals
Attends team meetings, taking notes on discussion points and action items-ensuring proper follow through
May work with clinical teams to create and distribute newsletters and communications to sites
Support, monitor, and analyze daily projects and contracts using Excel, Power Point, SCTMS, RAD, Vision Tracker, SharePoint, and shared network drive
Create, run, and monitor metrics and maintenance reports on an ongoing basis
Identifies issues in documents, memos, correspondences, and telephone calls which require action. Recommends alternatives and executes an alternative when appropriate
Support process improvements efforts to enhance systems and reduce lead time
Perform various study duties including facilities coordination, project document organization and reconciliation, setting up files, ordering supplies/equipment, photocopying
Solves problems of moderate scope and complexity following established policies and procedures
Works under limited supervision
Must Have (Minimum Requirements):
To be considered for this role, the minimum requirements must be evident on your resume.
Years of Experience:
Minimum of 6 years of administrative and/or project experience
Nice to Have (Preferred Qualifications):
Associates or Bachelors degree preferred
7+ years experience in clinical study administration or related experience
Clinical research/study coordination experience at Medtronic or medical device industry
Experience with Surgical Robotics products/therapies
Experience working with Siebel CTMS and Clinical RAD applications
Knowledge of medical terminology
Basic knowledge of GCP and regulatory compliance guidelines for clinical trials
Proficiency in MS Office applications: Excel, PowerPoint and Word, Project (or similar scheduling software), project management techniques and tools; and web-based applications.
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.
Physical Job Requirements:
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
For employees working in Quebec, Canada only: Basic knowledge of French is required. - (Quebec-Canada)
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Learn more about our benefits at benefits.medtronic.com
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.