Principal, Clinical Project Management
Johns Creek, GAFull-time
72K–108K a year
Behavioral Health Market Context
Apply Nowvia Talents By Vaia
Benefits
Health InsuranceDental CoveragePaid Time Off
Job Description
ulture and are looking for diverse, talented people to join Alcon. The Principal, Clinical Project Management role is pivotal in driving forward our mission of advancing eye care through development of next generation products. This position is location in Johns Creek, GA. A typical day will include: Crafting and providing oversight of clinical research programs Establishing relationships with key opinion leaders and applies their input to improve study design and protocols Confirming clinical research program design meets scientific objectives and is aligned with commercial needs Serving as medical/scientific consultant to marketing or research project teams and government regulatory agencies Establishing the criterion crucial for determining safety, efficacy, and medical utilities Interpreting results of Phase I to Phase III investigations in preparation for new-drug or medical device application Serving as the safety authority for individual clinical projects. Being responsible for post marketing studies. What you'll bring to Alcon: Bachelor's Degree or equivalent years of directly related experience (or high school +13 yrs; Assoc.+9 yrs; Bach. +5 yrs; M.S.+2 yrs; PhD+0 yrs) Proven ability to fluently read, write, understand and communicate in English 5 Years of Relevant Experience Travel Requirements: 10% Relocation assistance: Yes How you can thrive at Alcon: Collaborate with teammates to share standard processes and finding as work evolves. See your career like never before with focused growth and development opportunities. Join Alcon's mission to provide outstanding innovative products and solutions to improve sight, improve lives, and grow your career! Alcon provides robust benefits package including health, life, retirement, flexible time off and much more! ATTENTION: Current Alcon Employee/Contingent Worker If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site. Find Jobs for Employees Find Jobs for Contingent Worker 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.
Salary: USD 72000 - 108000 per year
Experience: 5 years required
Salary: USD 72000 - 108000 per year
Experience: 5 years required
Qualifications
- •What you'll bring to Alcon: Bachelor's Degree or equivalent years of directly related experience (or high school +13 yrs; Assoc.+9 yrs; Bach. +5 yrs; M.S.+2 yrs; PhD+0 yrs) Proven ability to fluently read, write, understand and communicate in English 5 Years of Relevant Experience Travel Requirements: 10% Relocation assistance: Yes How you can thrive at Alcon: Collaborate with teammates to share standard processes and finding as work evolves
- •Experience: 5 years required
Benefits
- •Alcon provides robust benefits package including health, life, retirement, flexible time off and much more!
Responsibilities
- •A typical day will include: Crafting and providing oversight of clinical research programs Establishing relationships with key opinion leaders and applies their input to improve study design and protocols Confirming clinical research program design meets scientific objectives and is aligned with commercial needs Serving as medical/scientific consultant to marketing or research project teams and government regulatory agencies Establishing the criterion crucial for determining safety, efficacy, and medical utilities Interpreting results of Phase I to Phase III investigations in preparation for new-drug or medical device application Serving as the safety authority for individual clinical projects
- •Being responsible for post marketing studies
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