What are the responsibilities and job description for the Clinical Project Lead I position at ASK Staffing?
Job Description:
Note : Experience with MDR remediation is Must.
Position Summary:
The contractor will be responsible/accountable for the following,
Act as the primary point of contact for the Clinical project lead and support in Life Cycle Management/Post Production Life Cycle Management activities
Provide clinical functional review and expertise on the assigned projects/tasks
Be responsible for timely authoring (as applicable), revisions, update, on clinical related documents for Medical Device Regulation (MDR) remediation and Post production Risk Reviews (PPRRs).
Review large documents such as literature reports, clinical research protocols, and review template documents as assigned by the project lead
Assist in literature review activities as assigned by the project lead and/or CDMA Franchise Head
Attend Clinical team meetings, and any other project meetings as assigned by the Project Lead and represent the function
Complete training activities to better understand product therapeutic area as assigned by the project lead
Proficient in European Medical device regulations
Experience in writing and reviewing medical and clinical evaluation documents
Experience in eye care/ophthalmology is preferred
Strong communication and writing skills
Master's or PHD in vision science or foreign trained Opthamologist.
About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities
ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.
Salary : $59,700 - $75,600