Stryker is one of the world's leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Clinical Study Associate to join our Joint Replacement Division in Mahwah, NJ.
Who we want
Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
Data translators. Highly effective communicators who can transform data findings into recommendations to compose reports and presentations.
What you will do
As a Clinical Study Associate, you will assist the Clinical Study Manager on the execution of multi-center national and international clinical trials within the Joint Replacement Division at Stryker. You will support the management of hip, knee and robotic clinical trials, with the opportunity to work on studies at various stages of study start-up, follow-up, and closure. You will strive for excellence in supporting the conduct of clinical trials, while monitoring and analyzing clinical data, focused on the primary goal of patient safety and satisfaction.
Support the conduct of one or more clinical trials, including Investigational Device Exemption, post-approval, post-market surveillance, feasibility, and/or marketing studies
Assist in executing clinical study protocols, timelines, and budget management
Collaborate with Clinical Operations Data Management on data collection, quality control and analysis of clinical trial patient data and radiographic results
Support the communication of study results through annual reports, investigator meetings, and global clinical discussions; track study performance through metric-based results
Ensure compliance of clinical trials with federal and applicable regulatory agency requirements, Good Clinical Practices, and Standard Operating Procedures
What you need
A Bachelor of Science Degree or equivalent focus is required
0-2 years of relevant experience
Basic knowledge and experience with Clinical Research either from an investigative site, Institutional Review Board (IRB) or sponsor preferred
Strong analytical and technical writing skills
Working knowledge of Good Clinical Practices (GCPs) preferred
Working knowledge of project management tools
Strong interpersonal, written and oral communication skills
Strong organization and planning skills
Demonstrated success in a team-based environment
Demonstrated knowledge and application of personal computer systems and desktop applications
Work From Home: No
Travel Percentage: Up to 25%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.
Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.