13 USA-Regulatory Affairs Specialist Project Lead I (Scientific) Jobs in Bridgewater, NJ
SORT BY
C
e
A
A
I
S
S
A
C
I
S
T
e
USA-Regulatory Affairs Specialist Project Lead I (Scientific)
$108k-140k (estimate)
Contractor | IT Outsourcing & Consulting
1 Week Ago
eTeam is Hiring an USA-Regulatory Affairs Specialist Project Lead I (Scientific) Near Bridgewater, NJ
Regulatory Affairs Specialist Project Lead I (Scientific)
6 Months extendable contract
Bridgewater- NJ- 100% Remote
Pay Range: $70-90/hr on w2Requires candidates that have worked on medicinal products (small molecule or biologic) marketing applications-- like NDA, BLA, MAA.
Fully Remote
This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development.
Additionally, this role leads the development of a global HA (Health Authority) interaction plan and strategy in collaboration with GRT (Global Regulatory Team) and is accountable for the communication of the key outcomes to senior management.
Education And Experience" BS/BA degree in a relevant scientific discipline required. Advanced degree (PharmD, PhD, MD or DVM or MSc in Biology, Life Science, or related field) is preferred.
" At least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development.
6 Months extendable contract
Bridgewater- NJ- 100% Remote
Pay Range: $70-90/hr on w2Requires candidates that have worked on medicinal products (small molecule or biologic) marketing applications-- like NDA, BLA, MAA.
Fully Remote
This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development.
Additionally, this role leads the development of a global HA (Health Authority) interaction plan and strategy in collaboration with GRT (Global Regulatory Team) and is accountable for the communication of the key outcomes to senior management.
Education And Experience" BS/BA degree in a relevant scientific discipline required. Advanced degree (PharmD, PhD, MD or DVM or MSc in Biology, Life Science, or related field) is preferred.
" At least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development.
Job Summary
JOB TYPE
Contractor
INDUSTRY
IT Outsourcing & Consulting
SALARY
$108k-140k (estimate)
POST DATE
06/19/2024
EXPIRATION DATE
07/17/2024
WEBSITE
eteaminc.com
HEADQUARTERS
SOUTH PLAINFIELD, NJ
SIZE
500 - 1,000
FOUNDED
1999
TYPE
Private
CEO
BIPIN TAHKUR
REVENUE
$50M - $200M
INDUSTRY
IT Outsourcing & Consulting
Related Companies
About eTeam
eTeam provides industry-specific, SOW-based services, and global contingent workforce managementsolutions.
Show more
Similar Jobs
Popular Articles
Top 10 Things to Avoid Putting on a Job Application
Read Article
How to Describe Your Education in a Resume
Read Article
How to Write a Memorable Cover Letter in 5 Ways
Read Article
4 Personal Finance Tips to Make During Job Transition
Read Article
4 Best Camera Setups for Interview
Read Article
Keeping a Job Search Journal: 9 Types of Journaling You Can Do
Read Article
