CMC Biochemistry Study Coordinator

  • Full-time

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

 In 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

The Study Coordinator role is mainly to assist Technical Group Leaders in auditing, correcting and controlling critical LIMS activities related to Study-based work. Responsibilities may include: 

  • Assist Technical Group Leaders with the auditing of LIMS entries for study-based work.
  • Assist Technical Group Leaders with the auditing of LIMS entries for routine testing (e.g. batch charges)
  •  Help ensuring that all pre-kick off documents have been provided to Clients and returned to ELLI with the appropriate information
  • Generate eJIRA tickets for all documentation pertaining to study-based work
  • Manage and is responsible for all CoA/Report corrections following QA rejection. If required, is responsible for liaising with the appropriate Technical Group Leader to address non-format related issues
  • Assist Technical Group Leaders by handling sample-related question typical to pre-kickoff and in-progress programs such as sample requirements, vialing requirement ,allocating needs etc…
  • Maintain and control Department-wide documentation such as Material requirement sheet.
  • Performs other duties as assigned

 

Qualifications

The Ideal Candidate Would Possess: 

  • Good oral and written communication skills
  • Independent work skills, strong work ethic and excellent Organization skills
  •  Attention to detail, ability to learn fast and work against timelines required
  •  Computer skills (expertise with MS Project, Excel, and other Windows related applications)
  • Ability to work on multiple projects at one time

Basic Minimum Qualifications: 

  • BSc in Science preferred but not required
  •  Understanding of complex Laboratory Management Systems preferred
  •  Experience in an FDA regulated Biotech/Pharmaceutical industry preferred

Additional Information

Position is full-time, Monday - Friday 8:00am - 4:00pm.  Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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