Job 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. 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.

Job Description

Primary Duties and Responsibilities:

1. Generate clinical study reports for studies conducted across multiple ECRL sites;
2. Incorporate and/or summarize aspects of the clinical study protocol, case report forms, review board documentation, data generated during the study, and statistical analysis into clinical study reports;
3. Interact with Laboratory Staff, Investigators, Statisticians, Project Managers and Quality Assurance Auditors from any or all of the ECRL sites to coordinate the assembly of data, documentation, methodology, and necessary revisions to clinical study reports;
4. Present and orient data in appropriate tables, figures or screenshots;
5. Write and review clinical study protocols, incorporating specifications of Investigators, Laboratory Staff, Statisticians and Study Sponsors;
6. Coordinate communication with the Laboratory Staff and Study Sponsors during the review of the clinical study protocol;
7. Uphold company-wide SOPs to ensure consistency and quality throughout protocols and reports;
8. Special projects as assigned by Technical Writing Manager.

Qualifications

• Ability to multi-task and discern the priority of tasks based on deliverables schedule.
• Adept computer knowledge i.e Microsoft Suite, Snipping Tool, Adobe or equivalent software
• Proficient with Microsoft Word, Excel and Outlook

Education and Experience:

• Bachelor’s degree
• At the discretion of senior management, additional experience may qualify an individual in place of a Bachelor’s degree

Additional Information

Schedule:

• Position is fully remote, Monday-Friday 8:00am-5:00pm

What we offer:

• 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 USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.

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