Research Regulatory Coordinator - (Full-time, Hybrid)
Virta HealthSalary not specified
- Full Time
- Junior (1 to 2 years)
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceutical, Clinical ResearchIndustries
Requirements
Candidates should possess a Bachelor's degree in life sciences or an equivalent educational background, along with relevant work experience in a clinical research environment or medical setting, such as a clinical research coordinator, Research Assistant, nurse, or medical assistant. They should have a good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules. Basic knowledge of medical terminology is required, and fluency in Dutch language is preferred. Strong IT competence, including proficiency in MS Windows and Office applications like Access, Outlook, Excel, and Word, is also necessary.
Responsibilities
The Clinical Research Coordinator will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator. They will maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents, support with screening and enrolment of patients and collection of related documents, plan and coordinate logistical activity for study procedures, perform data entry, data quality checking, and query resolution, manage and ship biological samples, conduct ECGs, take vital signs, and perform phlebotomy. Furthermore, they will coordinate with the study monitor on study issues and effectively respond to monitor-initiated questions and handle administrative research tasks.
Skills
Clinical Trials
CRFs
EDC Systems
Medical Terminology
MS Windows
MS Office (Access, Outlook, Excel, Word)
Data Entry
Data Quality Checking
Query Resolution
Phlebotomy
ECG
Biological Samples
IQVIA
Advanced analytics and clinical research services
About IQVIA
IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.
Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees