Clinical Research Feasibility Coordinator

🔥 10 hours ago

🐊 Florida – Remote

🐊 Florida – Remote

⏰ Full Time

🟢 Junior

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Alcanza Clinical Research

WebsiteLinkedInAll Job Openings

201 - 500 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Alcanza Clinical Research is a company dedicated to advancing clinical research through inclusive and impactful methodologies. They facilitate the participation of diverse populations in clinical trials by lowering barriers and ensuring high-quality research practices. Alcanza collaborates with medical providers and community organizations to provide patients with access to cutting-edge treatment options and health education across various therapeutic areas, without requiring insurance. Participants can benefit by receiving healthcare access, emerging treatments, and compensation for their time. The company is committed to patient safety and data integrity, providing opportunities for individuals to contribute to healthcare advancements across many locations in the United States.

📋 Description

• Process clinical research feasibilities for all sites according to sponsor/CRO timelines and requirements. • Review protocols or protocol synopses and study details to conduct feasibility assessments. • Identify potential investigators and site leaders in conjunction with the Business Development team. • Contact investigators and site leaders to discuss study details and assess study feasibility. • Maintain documentation of site capabilities and equipment, including MRI, PET, and CSF capabilities. • File completed questionnaires and relevant documents into the CRM. • Submit and update feasibility questionnaires. • Add per-patient budget amounts into systems. • Input principal investigator information into sponsor, CRO, and similar databases. • Back up completion and collection of signatures for confidential agreements. • Assist with management of the upcoming research trials pipeline and applications for new studies. • Complete company training, webinars, and required meetings. • Communicate and work with clients and internal and external stakeholders professionally and promptly. • Maintain confidentiality of patient, customer, and company information. • Perform other assigned duties.

🎯 Requirements

• A high school diploma or equivalent AND 2+ years of administrative, sales support, or similar experience, OR an equivalent combination of education and experience, is required. • 1+ years of clinical research experience is required. • Prior experience with the feasibility process in a clinical research setting is highly preferred. • Bi-lingual (English / Spanish) proficiency is a plus. • Proficiency with Microsoft applications, email, electronic health records, web applications, and proficient typing at 40+ wpm. • Ability to perform basic clinical procedures such as blood pressure, vitals, EKGs, and phlebotomy. • Strong organizational skills and attention to detail. • Well-developed written and verbal communication skills. • Well-developed interpersonal and listening skills; ability to work independently and with co-workers, subjects, managers, and external customers. • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities. • Professionalism, respect for others, self-motivation, and a strong work ethic. • High degree of integrity and dependability. • Ability to work under minimal supervision, identify problems, and implement solutions. • Ability to handle highly sensitive information confidentially and professionally, in compliance with HIPAA guidelines.

🏖️ Benefits

• Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.