Task Impetus Inc.
Overview
The Junior Clinical Research Coordinator assists, and implements clinical research projects at client. Under general direction, performs duties associated with coordinating study initiation, investigators’ training, and implementing study protocols. A clinical research coordinator (CRC) plays an integral role in medical studies of all kinds, usually under the direction of the principal investigator (PI). The CRC supports, facilitates, and organizes daily clinical trial activities and works with the department, sponsor, and institution to guide compliance, finances, and personnel issues. The CRC manages day-to-day clinical operations activities, overseeing and executing delegated tasks to appropriate parties.
Responsibilities
Overseeing the smooth running of clinical trials.
Collecting, coding, and analyzing data obtained from research.
Managing research budgets.
Informing participants about study objectives.
Administering questionnaires.
Monitoring research participants to ensure adherence to study rules.
Adhering to research regulatory standards.
Adhering to ethical standards.
Maintaining detailed records of studies as per FDA guidelines, including drug dispensation.
Liaising with laboratories regarding findings.
Participating in subject recruitment efforts.
Ensuring that necessary supplies and equipment for a study are in stock and in working order.
Engaging with subjects and understanding their concerns.
Analytical mindset and attention to detail.
Exceptional interpersonal, written, and verbal communication skills.
Excellent organizational skills and willingness to continually self-educate.
Qualifications
Bachelor or Master of Science in biotechnology, biochemistry, microbiology, biology, or an associate degree in nursing or related field.
Must have at least 1 year of work experience in healthcare.
Employment details
Seniority level: Entry level
Employment type: Full-time
Job function: Research, Analyst, and Information Technology
Benefits
Increment would be at least 15% every six months.
Relocation charges provided during the project.
Medical, dental, and vision benefits following 60 days of business.
401k retirement benefits plan following six months of work.
Other information
International candidates on OPT/CPT: Employer’s Confirmation Letter/CPT Letter/Offer Letter provided, to be submitted to your university within 90 days of OPT start. OPT Extension Letter provided for STEM extension eligibility. H1B sponsorship available once joining the client’s project.
Pre-job training with experienced trainers, assignments and case studies, mock sessions before interviews, multiple interview rounds with different clients, visa sponsorship, and training completion certificates.
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The Junior Clinical Research Coordinator assists, and implements clinical research projects at client. Under general direction, performs duties associated with coordinating study initiation, investigators’ training, and implementing study protocols. A clinical research coordinator (CRC) plays an integral role in medical studies of all kinds, usually under the direction of the principal investigator (PI). The CRC supports, facilitates, and organizes daily clinical trial activities and works with the department, sponsor, and institution to guide compliance, finances, and personnel issues. The CRC manages day-to-day clinical operations activities, overseeing and executing delegated tasks to appropriate parties.
Responsibilities
Overseeing the smooth running of clinical trials.
Collecting, coding, and analyzing data obtained from research.
Managing research budgets.
Informing participants about study objectives.
Administering questionnaires.
Monitoring research participants to ensure adherence to study rules.
Adhering to research regulatory standards.
Adhering to ethical standards.
Maintaining detailed records of studies as per FDA guidelines, including drug dispensation.
Liaising with laboratories regarding findings.
Participating in subject recruitment efforts.
Ensuring that necessary supplies and equipment for a study are in stock and in working order.
Engaging with subjects and understanding their concerns.
Analytical mindset and attention to detail.
Exceptional interpersonal, written, and verbal communication skills.
Excellent organizational skills and willingness to continually self-educate.
Qualifications
Bachelor or Master of Science in biotechnology, biochemistry, microbiology, biology, or an associate degree in nursing or related field.
Must have at least 1 year of work experience in healthcare.
Employment details
Seniority level: Entry level
Employment type: Full-time
Job function: Research, Analyst, and Information Technology
Benefits
Increment would be at least 15% every six months.
Relocation charges provided during the project.
Medical, dental, and vision benefits following 60 days of business.
401k retirement benefits plan following six months of work.
Other information
International candidates on OPT/CPT: Employer’s Confirmation Letter/CPT Letter/Offer Letter provided, to be submitted to your university within 90 days of OPT start. OPT Extension Letter provided for STEM extension eligibility. H1B sponsorship available once joining the client’s project.
Pre-job training with experienced trainers, assignments and case studies, mock sessions before interviews, multiple interview rounds with different clients, visa sponsorship, and training completion certificates.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr