Global Regulatory Affairs Project Director - Remote
- Employer
- Labcorp
- Location
- Athens, Greece
- Salary
- Competitive
- Start date
- 4 Sep 2022
- Closing date
- 3 Oct 2022
View more
- Discipline
- Quality
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
What to Expect
- Lead a team of Regulatory Project Managers providing a range of regulatory services to clients, both as standalone regulatory projects and as components of a broader engagement such as a clinical study.
- Manage larger or more complex regulatory projects, providing training and mentoring opportunities for staff.
- Manage project management metrics, project tracking, resource requirements, contracting, and revenue tracking
- Identify, promote and implement best practices for regulatory affairs driving for sustainable competitive advantage
- Assist with the development of proposals, including the development of proposal templates and associated costing tools
- Assist with the identification and selection of, and alignment and operations with partners
- Perform other duties as assigned by business unit leadership.
Education / Qualifications
- University/college degree (life science preferred), business, project management or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.
- Knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries.
- A good understanding of the drug development process.
Experience
- At least 10 years experience in the pharmaceutical industry with 7 years preferably in Regulatory Affairs or in Drug Development.
- Demonstrated skills and competency in project management tasks
- Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
- Broad knowledge of drug development process and client needs.
- Comprehensive understanding of processes associated with Global Regulatory Affairs activities
- Skilled in trouble-shooting and issue resolution
- Strong interpretation and analytical skills within and across projects / portfolios leading to documented efficiency improvements
- Ability to lead diverse cross-functional teams and deliver measurable results
- Experience in managing a project budget with documented cost containment strategies.
- Ability to work with minimal supervision.
- Excellent communication, facilitation and presentation skills
- Good conflict management skills
- Good computer skills with a working knowledge of a range of computer applications.
- Excellent planning, time management and organization skills.
- Ability to work efficiently and effectively in a matrix environment.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement .
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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