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Clinical Operations Lead Jobs

Company

Alcon

Address United States
Employment type FULL_TIME
Salary
Category Medical Equipment Manufacturing
Expires 2023-06-29
Posted at 11 months ago
Job Description
Are you ready to see your future like never before? If so, Alcon is the place for you! A career at Alcon is like no other. We are innovative. We are impactful. We are the largest eye care medical device company helping restore sight and allowing millions of people worldwide to see brilliantly. We have a long history of industry firsts and a diverse hardworking team that keeps us on the cutting edge.


We are currently hiring a Clincial Trial Lead to join our U.S. Development Medical Device Trial Management team. This person will oversee and resolve operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets.


Job Title: Clincial Trial Lead


Location: U.S. Remote


Key Responsibilities:


  • Initiate Investigational Product shipment requests, resupply and coordinate reclamation of supplies for sites on assigned trial(s)
  • Lead project to support a team of Clinical Site Managers (CSMs) for assigned trial(s), tracking site progress, achievements, and status of CSM activities
  • Proactively identify potential/actual issues and risks, bring up to management as appropriate, and contribute to mitigation
  • Create and maintain user account worksheets for provisioning all site personnel for assigned trials into required systems (e.g., EDC, IRT, training portals)
  • Prepare, coordinate, deliver, and track protocol specific training
  • Develop Protocol Monitoring Plan (PMP)
  • Lead the site management team responsible for operational activities for study/site activation, conduct, and close-out of 2-3 clinical trials of low to medium complexity in support of one or more projects.
  • Provide operational feasibility/site management input to the development of the protocol, manual of procedures, informed consent template and data validation plan.


Key Requirements/Minimum Requirements


  • Sponsorship available: No
  • The ability to fluently read, write, understand, and communicate in English
  • 5 Years of Relevant Experience
  • Bachelor’s Degree or Equivalent years of directly related experience (or high school +13 yrs; Assoc.+9 yrs; M.S.+2 yrs; PhD+0 yrs)
  • Work hours: 40
  • Relocation assistance: No
  • Travel Requirements: Like domestic or international (Percentage)


Preferred skills:


  • Ophthalmology background
  • Direct experience with Clinical Research, operations, and Management
  • Experience with leading teams


Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to [email protected] and let us know the nature of your request and your contact information.