Job Description

Reference # : 18-03718Title : CMC Documentation Analyst
Location : Pennington, NJ
Position Type : Contract
Experience Level : Start Date / End Date : 04/23/2018 / 10/22/2018
Assignment Detail
Industry:Biotech/PharmaJob Category:Administration / Customer Service
Description
CMC Documentation Analyst


Work for a global healthcare leader. Eclaro is looking for a CMC Documentation Analyst for our client located in Pennington, NJ.
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!

JOB DESCRIPTION:

The primary role is to support the documentation activities for regulatory submissions for biologic products as part of the CMC Strategies team. The CMC group is committed to supporting the biologics network with integrity, reliability, active engagement and cross-functional collaboration.

Duties and Responsibilities:
  • Support the logistical process for regulatory submissions including pre and post submissions while interfacing across the Pharmaceutical Client network.
  • Assist with dossier creation and system compliance for regulatory submissions.
  • Assist in the facilitation of authoring, review, verification and submission-ready compliance for the finalization of filings.
  • Participate in initiatives involved with regulatory filings.
  • Participation on various cross-functional project teams, interactions with MS&T, TPT, IDT, SLT and GRS-CMC staff at different BMS sites and other key partners both internal and external to the company are necessary.
  • Must possess the ability to support multiple projects and to prioritize work independently.
  • Work in a team environment and foster teambuilding for the improvement of processes and enhancement of productivity to align with key business drivers.
  • Demonstrate commitment to excellence and bring a high energy level to daily activities as well as involve periods of high intensity work under tight timelines.
QUALIFICATIONS:
  • BS degree required. 1-2 years of direct pharmaceutical work experience preferred. Advanced degree is an asset.
  • Excellent organizational, communication and project management skills are required along with proficient navigation of electronic systems.
  • Must demonstrate an understanding of the global CMC regulatory guidelines, practices and applications.
  • Must have a working knowledge of regulatory submissions for pre and post filings.
  • Ability to successfully collaborate with a diverse group of technical professionals and interpersonal styles is required.
  • Must be capable of working in a fast-paced changing team environment, prioritizing multiple tasks to meet filing deadlines and ensuring the most efficient regulatory process.
  • Possess strong interpersonal skills and demonstrates ability to effectively interact with business functions.
If interested, you may send your resume to:
Cheryl.Buot@eclaro.com

https://www.linkedin.com/in/cheryl-buot-56ba4836


If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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