Clinical Support Specialist

About us

We are in the animal health business, partnering with our clients in the areas of Research and Development (R&D) and manufacturing to produce pharmaceuticals for both farm and companion animals. Originally founded in 2006 by a New Zealand chemist with an entrepreneurial mindset, Argenta's vision is "Healthier Animals, Sustainably". Our recipe for success has been our uniqueness in our vision and our people. Argenta now has operations across the globe with locations in New Zealand, the United States, Scotland, Germany, and Spain with 600+ employees globally.

Argenta is currently looking to fill the role of Clinical Support Specialist in the Lawrence, Kansas location.

About the role

Collaborates in the review of study records and all study notebooks to ensure contents are current and complete.

• Assists in providing tracking and Quality Control (QC) of data as required and assists with responses to QA audits.
• Utilize Good Clinical Practice (GCP) to complete assigned tasks.
• Assist the Clinical team with designated tasks (protocol/form development, SOPs, tables/listings for Final Study Report, etc.) that support the timely completion of the projects assigned to the specialist.
• Scan, bookmark, maintain Central Files including organization and filing of documents (i.e. paperwork related to the study specific documents).
• Work with Project Managers to determine study start up.
• Facilitate and create/QC of study materials, g., study notebooks, computer tablets, Owner folders, etc.
• Assist in shipment of study materials, study documentation, electronic data, to Sponsor at study completion.
• Provide miscellaneous administrative support, g., answering telephones, scanning documents, filing, preparing FedEx shipments, photocopying, etc.
• Support and shadow Clinical Research Associate(s) with specific tasks during initiation, interim, and close-out visits.

• Follows established standard operating procedures and/or study specific data management plan using an internal database or electronic data capture.
• Perform first and second data entry while utilizing science/veterinary background to ensure high quality of dataset.
• Review Project needs with Project Manager and coordinate tracking and study support resources.

Requirements:

• Bachelor's degree or equivalent experience in a scientific discipline
• Proficient use of Microsoft Office Products, capable of learning new system related programs Outstanding accuracy, attention to detail, and organizational skills
• Quality interpersonal, communication and presentation skills; verbal and written communication with internal and external stakeholders must be clear and concise
• Action and results oriented with strong problem-solving skills
• Capable of working in a changing environment and under pressure
• Gathers key information essential to the planning and process of clinical trial management
• Works collaboratively with key stakeholders to streamline operations for maximum efficiency, automation, and effectiveness where appropriate
• This role will train in the New Brunswick, NJ location. The candidate must be willing to spend time in the office learning the role. Detailed training schedules will be shared at offer

Why us?

Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through strong culture, great benefits, and opportunity for growth.

This position does report to the office daily.

To find out more about Argenta, click here: www.argentaglobal.com