Clinical Research Coordinator (80808)


As a clinical research coordinator, Proficient in coordinating all phases of clinical trials, including protocol review, regulatory compliance, and site management.Also Proficient in data collection, entry, and management. Ensure accuracy and completeness of study data while adhering to SOP .


  • Coordinating and overseeing the running of clinical trials
  • Recruiting and screening participants for trials
  • Managing documents and records of participants and trials 
  • Ensuring trials are delivered following regulatory, government, and ethical regulations and requirements
  • Ensuring the safety of participants, supplies, and materials
  • Performing cost analysis and preparing budgets
  • Designing and delivering training to staff and participants 
  • Collecting data and maintaining detailed records
  • Acting as a point of contact for study participants to ask any questions or express concerns 
  • Promoting the study through meetings, events, and seminars
  • Overseeing the research team


A bachelor’s degree in a related field such as life sciences, nursing, pharmacology, or a health-related discipline is often required.
Some positions may prefer or require a master’s degree in clinical research, public health, or a related field.
5-6 years experience working in clinical research is highly beneficial.
Familiarity with the Code of Federal Regulations (CFR) and International Conference on Harmonisation (ICH) guidelines is often required.
Strong communication skills are crucial for interacting with diverse stakeholders, including study participants, healthcare professionals, and research team members.


Taskimpetus Inc.




  • Increment would be at least a minimum of 15% every six months.
  • Relocation charges will be provided to you during your project
  • Medicinal, Dental and Vision benefits following 60 days of business.
  • Medical coverage qualified following 60 days of business.
  • Present moment and long-haul handicap following 60 days of work.
  • 401k retirement benefits plan qualified following half a year of work.

Only for international candidates on OPT/CPT:

  • Employer’s Confirmation Letter/CPT Letter/Offer Letter will be provided, which you need to submit to your university within 90 days of the start of your OPT.
  • OPT Extension Letter will be provided to those candidates who are qualified for STEM extension.
  • H1B Sponsorship will be provided to OPT and CPT candidates only once they join our client’s project.

Other Benefits:

  • Pre-job Training with Experienced Trainers.
  • Assignments & Case Studies provided during training.
  • Mock sessions before interviews
  • Multiple interview rounds with different clients.
  • Visa Sponsorship
  • Training completing certificates
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