JobWatch

22 days old

Regulatory Affairs Specialist

Kelly Services
Titusville, NJ 08560
Kelly Scientific is leading a search for a senior **Regulatory Affairs Specialist** to help spearhead the initiatives of an established and growing biopharmaceutical firm.


+ Title: **Sr. Regulatory Affairs Specialist**

+ Location: Titusville, NJ (08560)

+ Duration: 6+ months


Regional Strategic Implementation (RSI) is part of the Regional Regulatory Affairs organization within Global Regulatory Affairs and supports regulatory activities in Asia Pacific (AP), Latin America (LA) and the Emerging Markets of EMEA. The team efficiently and effectively executes regional strategies and leverages processes and resources across all regions. We are therapeutically aligned and support the full lifecycle of products in all therapeutic areas.


**Scope of Responsibilities:**

The Sr. Regulatory Affairs Specialist, Regulatory Strategic Implementation (RSI) will:

For Marketing Authorization Applications, provides regulatory support throughout registration process and life-cycle management (e.g. iCTDs, ACTDs, renewal applications, Health Authority Responses, site registrations and routine marketed product submissions including PSURs, RMPs).

Advises team on required documents in preparation of submissions as assigned in collaboration with RSI Lead.

Assists with timely registration dossier availability, ensures that all document components are in place on time, identifies and tracks critical path activities.

Compiles Module 1 for iCTDs to be dispatched to countries.

Manages and tracks the assembly of country-specific submission packages to the LOCs in accordance with agreed plans.

Participates in Working groups to ensure timely regional and local input into product objectives, to align regions with CDT/Global strategy.

Interacts with the regional teams and Local Operating Companies to support regional and local activities.

Drafts and reviews document content (depending on level of regulatory knowledge/expertise);

Provides input to documentation to ensure they are in line with product strategy and thoroughly and accurately answers the questions being posed;

Identify and initiate on-going continuous process improvement opportunities with end users responsible for data entry and/or data consumption.

Advises team on required documents in preparation of Clinical Trial Applications (CTA)

Provides operational support for the assembly and distribution of submissions ( e.g., CTA for China, Health Authority Responses).

Support projects related to improved system functionality or to develop new business capabilities.

Responsible for the critical review of submission documents to ensure compliance with regulatory requirements.

Provides regulatory support for and appropriate follow-up to inspections, audits, litigation support and product complaints (depending on level of regulatory knowledge/expertise).

Serves as the Regulatory representative on specific multi-discipline teams.

Keeps abreast of current and pending approvals in specific therapeutic areas and is knowledgeable of laws, guidance and requirements related to those areas.

Contributes to process improvement initiatives within and across functions.


**Qualifications**

B.A./B.S. in science/relevant health-related discipline with a minimum of 4 years of relevant experience.

Basic understanding of the product and registration life cycle from global regulatory affairs, local operating company or affiliates, and submission process perspectives is required.

Knowledge of external factors (standards, regulatory requirements) that impact Product & Lifecycle Registration is preferred.

Previous experience liaising with local, regional, and central regulatory users to ensure that new and ongoing regulatory requirements are reflected in the system configuration, functionality and business processes is highly preferred

Demonstrated ability in working in global project teams in a matrix environment across multiple projects is required.

Demonstrated ability to handle multiple projects.

Must have experience developing and maintaining strong relationships.

Must have strong collaboration skills in order to partner effectively across other business units.


**Why Kelly** **** **?**


Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.


**About Kelly** ****


At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. (https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm)

Categories

Posted: 2021-05-21 Expires: 2021-06-21

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Regulatory Affairs Specialist

Kelly Services
Titusville, NJ 08560

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast