Staff Clinical Trial Specialist
Staff Clinical Trial Specialist
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$ 105000 - 165000
1 Vacancy
Job Description
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at
Job Function:
Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:
Clinical Development & Research Non-MDJob Category:
Scientific/TechnologyAll Job Posting Locations:
Irvine California United States of America Jacksonville Florida United States of AmericaJob Description:
We are searching for the best talent to join our Vision team as a Staff Clinical Trial Specialist located in Jacksonville FL or Irvine CA.
Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments Ready to join a team thats reimagining how vision is improved Our Vision team solves the toughest health challenges. Help combine cutting-edge insights science technology and people to encourage eye care professionals and patients to proactively protect correct and enhance healthy sight for life. Our products and services address these needs from the pediatric to aging eye in a patients lifetime.
You will:
- Own processes and information required to complete and support the clinical trial including clinical trial project plan project timelines resourcing budget plans and statements of work
- Accountable for the preparation and finalization of key clinical documents which include the informed consent case report forms and other essential study documents
- Manage study conduct ensuring that operating procedures and company policies are followed and that trials meet all applicable Regulations and Guidelines required for testing investigational and/or marketed devices
- Responsible for the selection of Contract Resource Organizations (CRO) and oversight of contracts timelines and budgets when applicable
- Contribute to the improvement of clinical trial processes including benchmarking and maximizing across other J&J companies
- Other related duties as assigned by management
Qualifications:
- Bachelor of Science or equivalent degree
- 5 years experience in Clinical Research in a medical device or pharmaceutical regulated industry
- Must have a minimum of 2 years experience as a clinical research associate
- Complete understanding and application of principles concepts and practices of clinical research procedures and Good Clinical Practice (GCP)
- Strong communication organizational and interpersonal skills
- Basic understanding of diverse areas of business (e.g. R&D Operations QA laboratory regulatory project management etc.)
- Ability to effectively work with a team and influence peers affiliates and Regulatory agencies (primarily IRBs/Ethics Committees) to ensure that regulatory and business needs are met
#LI-AM2
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.
The anticipated base pay range for this position is :
$105000-$-165000Additional Description for Pay Transparency:
Subject to the terms of their respective plans employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical dental vision life insurance short- and long-term disability business accident insurance and group legal insurance. Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Companys long-term incentive program. Subject to the terms of their respective policies and date of hire Employees are eligible for the following time off benefits: Vacation 120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington 56 hours per calendar year Holiday pay including Floating Holidays 13 days per calendar year Work Personal and Family Time - up to 40 hours per calendar year Parental Leave 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave 10 days Volunteer Leave 4 days Military Spouse Time-Off 80 hours Additional information can be found through the link below. Experience:Staff IC
Employment Type
Full-Time
Key Skills
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