Senior Clinical Scientist

Full Time
Remote
Posted
Job description

Title: Clinical Evaluation Lead-VERY HIGH PRIORITY

Customer: Alcon

Location: Remote

Type: SC/FTE

Clinical Evaluation Lead engineer

Updates from the client-

We need to look for candidates who are researchers in Ophthalmic/optometric and have publications. (OD’s/Scholars/Doctorate degree (Ph.D)-Mandatory).

Please do not submit candidates who have only skills in Optometry.

Here are some schoolings/research areas/project’s role that we can source for: (These are the projects of the same candidate)

B.S. Optometry, Elite School of Optometry, affiliated with Birla Institute of Technology and Science, Pilani, India

B.S. Optometry, Elite School of Optometry, affiliated with Birla Institute of Technology and Science, Pilani, India

Ph.D. Vision Science, School of Optometry and Vision Science, University of Waterloo, Canada

Post-Doctoral Scholar, Department of Psychology, University of Nevada, Reno

doctoral Researcher, School of Optometry and Vision Science, University of Waterloo, Canada

Graduate Researcher, Elite School of Optometry, India

Project mentor and lead, Elite School of Optometry, India

optometrist, Sankara Nethralaya, Medical Research Foundation, India

Student Researcher, Elite School of Optometry, India

Skills: OD in optometry (scholars/ph.d)-mandatory, we need candidates as researchers in optometry

Job Description:

Qualifications

  • Ophthalmic/optometric expertise strongly preferred. Clinical trial background is advantageous.

Role profile

  • Attend Clinical team meetings, Clinical Sub team and Trial Team Meeting and any other project meetings as assigned by the Project Lead/Line Manager and represent the function
  • Activities include but not limited to, understanding, and putting together project plans, protocol synopsis, leading study plan/conduct/reporting activities (all aspects of the clinical
  • trial)
  • Lead Clinical Sub team meetings, work with a cross functional team and review study designs and formulate research questions/hypotheses.
  • Act as the primary point of contact for the portfolio Clinical project lead and provide support in Life Cycle Management/Postproduction risk review activities as needed
  • Provide clinical functional review and expertise on the assigned projects/tasks
  • Be responsible for timely authoring (as applicable), revisions, update, on clinical related documents
  • Review large documents such as literature reports, clinical research protocols, and review template documents as assigned by the project lead/line manager
  • Assist in literature review activities as assigned by the project lead and/or CDMA Franchise Head
  • Complete training activities to better understand product therapeutic area as assigned by the manager

Job Types: Full-time, Contract

Salary: $70,188.12 - $130,920.87 per year

Schedule:

  • 8 hour shift

Education:

  • Doctorate (Preferred)

Work Location: Remote

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