Clinical Support Specialist

At Argenta, we’re more than a company — we’re a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it.

Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.

We’re in a unique position. We are the world’s only combined contract research and contract development and manufacturing organisation (CRO/CDMO) dedicated to animal health.

Our uniqueness means:

• We are ambitious, growing and building a ‘one team’ culture, guided by our values.
  • We are team players;
  • We are doers;
  • We are customer-centric;
  • We are innovators.

We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best “paw” forward we will make the lives of the animals we care for, better.

With bases in New Zealand, the US, the UK and Europe, our 650+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let’s Make It Happen, Together.

TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply. 

Our US Clinical team is looking for motivated, driven individuals who thrive in their ability to multitask to join our team as a Clinical Support Specialist at our Shawnee, KS facility. 

The Clinical Support Specialist provides value through the following responsibilities: 

• 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.
  

Job 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
  

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 role is subject to a DEA background check as well as a pre-employment drug screen and/or physical.

Argenta is an equal opportunity employer

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

The position is in office Monday - Friday.  Overtime hours are required when necessary.

Equal Opportunity Employer