Clinical Research Staff, Paramedic

February 13

🦌 Connecticut – Remote

Although this job is listed in Connecticut, this company may be open to hiring remote in other states.

⏰ Full Time

🔴 Lead

🧪 Clinical Research

🦅 H1B Visa Sponsor

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Parexel

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Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

📋 Description

• Owns, maintains, and ensures clinical training transcripts are up to date at all times. • Maintains proficiency in various clinical procedures required in study execution. • Ensures clinical research studies are conducted according to protocol requirements and internal SOPs, guidelines, work instructions, and process maps. • Provides basic first aid and medical/nursing care within scope of practice. • Assists in sample management, collection, and generation of computer labels. • Records adverse events with referral to medical or nursing personnel for evaluation & treatment. • Performs electronic and diagnostic measurements including audiograms, electrocardiograms, visual exams, and other novel devices. • Performs and records physical measurements including vital signs and body measurements. • Creates volunteer identification (photos, badges). • Provides necessary instructions to research participants. • Monitors and maintains usage of daily clinic supplies. • Maintains equipment log & calibration records. • Creates and ensures quality in work and data output by performing data cache review. • Attends various clinical meetings (i.e. study start-up, in-service, department meetings, etc.). • Supports other additional clinical functions. • Demonstrates holistic understanding of work processes at the Unit. • Identifies with overall goals of the NHCRU and progresses clinical research studies as planned. • Assists in the overall planning and delivery of clinical trials. • Assists in the delivery of improved training program. • Leads/supervises clinic pCROs (and colleagues, as appropriate) during various shifts of operation as required. • Provides/ supervises clinic support activities such as scheduling (e.g., bed space, volunteer, staffing), supply requisitions and training, as required. • Collaborates with clinical coordinators and clinical floor leads to maximize study implementation.

🎯 Requirements

• Preferred Associate in Science degree in Life, Biomedical, or Social Science. • Bachelor of Science in a health-related field desirable. • Preferred qualifications include minimum of 1-2 years of work experience in clinical research trials as data collector or clinical coordinator. • State of Connecticut licensure as EMT-P. • Quality conscious with high degree of ethics and integrity carrying out duties in accordance to laws, regulatory standards, and with company policies and procedures. • Proficiency in Microsoft (MS) Office and the ability to learn different software programs. • Current certification in Basic Life Support (BLS) and Advanced Cardiovascular Life Support (ACLS) required. • Ability to work beyond normal work hours and various shift availability required.