Clinical Research Coordinator at Eurofins

Piscataway, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

14 Oct, 26

Salary

20.0

Posted On

16 Jul, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Clinical Study Conduct, Data Entry, Data Review, Time Management, Communication, Clinical Study Evaluations, ICH GCP Compliance

Industry

Medical and Diagnostic Laboratories

Description

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It 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. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Pay Range: $20.00/Hr. Shift: Monday- Friday, 9:30am- 6:00pm Primary Duties and Responsibilities of a CRC Act as project manager on studies as directed by department manager. Assist in the conduct of clinical studies as specified by the study protocol under the supervision of designated Principal Investigator and departmental management. Record observations, measurements, and test results, as required. Provide a professional experience to test subjects, and answer all inquiries, as appropriate Assist in the preparation of test materials, as needed. Perform data entry and data review to ensure study quality. Conduct studies in accordance to ECRL Standard Operating Procedures study protocol and ICH GCP. Efficiently time manage multiple projects. Succinctly communicate day to day project details to both department manager and Principal Investigator. Perform department specific procedures as qualified by training and evaluation of proficiency (clinical study evaluations and measurements) Process study data and prepare for reporting and conclusions. Qualifications High School Diploma Additional Information 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. Compensation: USD 20.00 - USD 20.00 - hourly

Responsibilities

The Clinical Research Coordinator acts as a project manager for clinical studies, ensuring they are conducted according to protocols and SOPs. Responsibilities include recording test results, managing data entry, and communicating project details to the Principal Investigator.