Senior Clinical Study Manager in Virtual, New Jersey at Stryker Corporation

Date Posted: 11/2/2018

Job Snapshot

Job Description

Who we want

Collaborators.  Collaborates and builds relationships with internal and external stakeholders

Achievers. Thrives on accomplishing tasks and constantly driven to do more

Communicators. Articulates well and expresses ideas effectively

Teammates.  Partners who listen to ideas, share thoughts and work together to move the business forward

Professionals.  Committed to quality and integrity

What you will do

We are looking for a solutions-focused team player who is prepared to take on a challenging role in the conduct and management of clinical research. As a Clinical Study Manager, you will interact directly with institutions and investigators, and will drive research initiatives and ensure alignment with strategic goals. You will be responsible for tasks that require a high degree of attention to detail and accuracy. You will be working with an international team of colleagues and investigators who are driven to deliver high quality results that make an impact on the quality of healthcare around the world.

  • Work in a virtual team environment, requiring that you be highly engaged, communicate effectively and maintain accurate and timely tracking and documentation
  • Take lead roles in the development and execution of studies designed to support clinical evidence of device safety and performance
  • Demonstrate excellent organizational, decision-making, and time management skills in a fast-paced environment
  • Build and maintain excellent working relationships with KOLs and colleagues
  • Coordinate and execute research projects, including clinical study plan and protocol development, contracting, auditing and monitoring, and close-out activities
  • Ensure operational aspects of the studies are being conducted in accordance with all relevant ethical and government standards, GCPs, and Stryker Standard Operating Procedures.
  • Maintain a high level of professional expertise through familiarity with scientific literature, product portfolio, and the competitive and healthcare environments.

What you need

  • Bachelor’s Degree in Health Sciences or other related technical discipline
  • 3+ years’ experience as a Clinical Research Associate, Clinical Project Manager or other related professional role
  • Fundamental knowledge and good understanding of GCPs, clinical trial design, study development and project management
  • Demonstrated interpersonal, written and oral communication as well as organizational planning skills

Work From Home: Yes

Travel Percentage: Up to 50%

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.

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