Clinical Research Coordinator

Overview

Do you want to watch clinical development change, or do you want to be the one to be a player in it?

We’re hoping you’re here for the latter.

Who are we?

We Are Elixia Clinical Research Collaborative.

We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real, and we see it every single day. We help get life-saving drugs into the hands of those who need them most.

Who are you?

Are you a recent grad looking for experience? Or maybe looking to use your skills in an ever-changing environment? Or a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Assistant in our Clinical Research Organization is the career for you!

Skills/Qualifications:

• Ability to work in a fast-paced environment.
• Able to multitask.
• Excellent ethical standards, conduct, and GCP compliance
• Self-motivated, willing and able to learn new knowledge and skills.
• Excellent organizational and communication skills
• Reliable, responsible, and accountable
• Flexibility in work schedule when possible must be maintained to ensure coverage of study responsibilities.
• Respect for patients and co-workers
• Bilingual – a plus
• Excellent computer skills
• Must know Phlebotomy

Responsibilities:

• Interact with study patients, including participate in the informed consent process, Schedule subject visits and procedures.
• Subject recruitment and executing study visits.
• Phlebotomy, obtaining medical history and vital signs, EKG, etc.
• Timely completion of all study visits procedures and documentation
• Collect, process and ship laboratory specimens.
• Dispensing study drugs, maintaining accountability. CRF completion
• Complete case report forms (paper & electronic data capture) and address queries.
• Support the safety of clinical research patients/research participants.
• Report adverse events.
• Understand good clinical practice (GCP) and regulatory compliance.
• Comply with company policies, standard operating procedures (SOPs) and guidelines.
• Facilitate pre-study, site qualification, study initiation, and monitoring visit.
• Retain records/archive documents after study close out.
• Traveling may be required

Required experience:

• One (1) year of clinical experience
• Previous Clinical Research experience preferred
• Phlebotomy Experience

Benefits

We passionately believe that our employees are the heartbeat of our organization and we are happy to offer the following benefits:

• Health insurance
• Dental Insurance
• Vision Insurance
• Life Insurance
• Employee Assistance Program
• Benefit eligibility is dependent on employment status.

To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

The Company is an equal opportunity employer and does not discriminate based on race, religion, color, national origin, age, sex, gender, sexual orientation, disability, or any other characteristic protected by law. You must be able to perform the essential functions of the position satisfactorily. Reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of this job, absent undue hardship.