**Seeking a Clinical Research Coordinator in Worcester, MA**
-MUST be able to perform phlebotomy!
Job Summary
We are a growing integrated research organization dedicated to bringing innovative care to patients across the U.S. The CRC is responsible for the day-to-day operations of clinical trials at the site which include coordinating participant visits, recruiting and retaining trial participants, and performing tasks as delegated, required to complete a study according to the protocol and ICH-GCP guidelines.
Key Responsibilities
Under the direction of the Senior Director of Clinical Research and the Principal/Sub
Investigator(s):
o Coordinates with Principal Investigator and local site to ensure that clinical research trials and activities are performed in accordance with the study protocol, FDA, GCP, ICH Guidelines and SOPs.
o Adhere to clinical trial protocols and coordinate and perform assigned clinical trial activities including, but not limited to:
o Participant pre-screening, recruitment and scheduling
o Complete protocol and trial system training
o Maintenance of regulatory documents
o Conducts or participates in the informed consent process and discussions with trial participants, including answering any questions related to the study.
o Conducting participant visits
o Ability to perform basic lab and clinical procedures per protocol, such as:
o blood specimen collection (phlebotomy)
o blood pressure
o vitals
o EKGs
o centrifuge operation
o storing and shipping of lab specimens
o accountability of specimens and notification of courier for specimen pick-up
o Entering data in the EDC and resolving all queries
o Updating and maintaining trial logs and participant charts
o Conducting monitoring visits and resolving issues as needed in a timely manner
o Managing and reporting of AEs, SAEs, and deviations
o Maintains adequate inventory of study supplies
Qualifications
o College degree (health sciences) preferred or significant relevant experience
o At least 2 years of CRC experience in a direct patient care role
o Knowledge of Good Clinical Practice (GCP), IATA and FDA regulations pertaining to clinical trials
o Fluent in written and spoken English
o Ability to complete clinical procedures including phlebotomy, vitals, height, weight,
ECGs
...can change lives and create lasting hope! Position: Registered Nurse Job Type: Full-Time / Non-Exempt Shift Details: Shift... ..., Saturday, and every other Wednesday 7:00 AM-7:30 PM Shift Nights- Thursday, Friday, Saturday, and every other Wednesday 7:00 PM-7...
...~ Approve all change orders ~$50K; oversee project scope, schedule, and budget ~ Manage a team of 810 (engineers, designers, BIM leads, EITs)~ Conduct quarterly profitability reviews; maintain 18% gross margins ~ Drive business developmentbring in new clients...
...Job Title: PLM System Data Entry Specialist (Temporary) Location: Commerce, CA (Hybrid) Schedule: 30-40 hours per week for 2-3 months; preferred hours are 9 AM - 3 PM Position Overview: We are seeking a detail-oriented Data Entry Specialist to support the implementation...
Job Details Comp: $41.50 The Radiology Technologist performs x-ray scans of patient's internal anatomy to aid physicians in diagnosing illnesses, diseases, or injuries. Executes radiologic services in compliance with relevant laws and regulations and provides consultation...
...Operate and care for production and support equipment, including: Reactors & thermal systems: Jacketed/stirred vessels, thermal oil systems, heat exchangers, condensers, chillers. Thermal processing: Ovens and furnaces for carbon/graphite processing; controlled...