Job Description

Documentation Analyst
Job Number: 21-07516
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Documentation Analyst for our client in New Brunswick, 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!

Position Overview;
  • The primary role is to support the documentation activities for regulatory submissions for biologic products as part of the client's Strategies team.
  • The group is committed to supporting the biologics network with integrity, reliability, active engagement and cross-functional collaboration.
  • Support the logistical process for regulatory submissions including pre and post submissions while interfacing across the 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 other departments and staff at different Client 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.
  • 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 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
If interested, you may contact:
Jay Lucas
Jay Lucas | LinkedIn
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

Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!

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