Operations Coordinator I / Daytona Beach, FL (On-Site)

United States·Daytona Beachmid

OperationsOperations Coordinator

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Quick Summary

Key Responsibilities

Responsible for practical/administrative activities in support of a clinical research trial.

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OperationsOperations Coordinator

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Operations Coordinator I, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)

This is a full-time, office/clinic-based job in Daytona Beach, FL.

If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.

WHAT YOU WILL DO:

Responsible for practical/administrative activities in support of a clinical research trial. The Operations Coordinator II supports and assists the senior study team members such as the Clinical Research Coordinator and Project Manager as appropriate.

Responsibilities

~2 min read

→University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
→In lieu of a degree, typically 2 years’ experience in related fields (e.g., pharmaceutical, laboratory, data analysis) will be considered in addition to the experience requirement.
→1-2 years of professional work experience with at least one year’s experience in clinical research.
→Basic knowledge of computers and programs (e.g., Microsoft Word, Excel).
→Knowledge of drug development process, ICH Guidelines and GCP.
→Basic Life Support Skills (BLS) or CPR/AED Certified.

The important thing for us is you are comfortable working in an environment that is:

→Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
→Changing priorities constantly asking you to prioritize and adapt on the spot.
→Teamwork and people skills are essential for the study to run smoothly.
→Technology based. We collect our data directly into an electronic environment.

What do you get?

→Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
→Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
→401(K)
→Paid time off (PTO)
→Employee recognition awards
→Multiple ERG’s (employee resource groups)

Physical Requirements:

→Ability to work in an upright and /or stationary position for 6-8 hours per day.
→Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
→Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
→Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
→Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
→Regular and consistent attendance.
→Varied hours may be required.