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Clinical Research Coordinator

0-5 years
Not Disclosed
12 June 4, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, ICD-10 CM, CPT, HCPCS Coding, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About the job

Company Description

 

NovoBliss Research® is a Contract Research Organization (CRO) located in Ahmedabad-Gandhinagar, India. Our spacious 10,000 sq. ft. facility is dedicated to advancing scientifically evidence-based products in cosmetics, OTC items, cosmeceuticals, and personal care. As a specialized CRO, we conduct trials in diverse industries, including Nutraceuticals, Dietary Supplements, Dermatology, Pharmaceuticals, Cosmetics, and Personal care.

 

Role Description

 

This is a full-time on-site role for a Clinical Research Coordinator at NovoBliss Research Private Limited. The Clinical Research Coordinator will be responsible for coordinating and managing clinical research studies, including activities such as informed consent, protocol adherence, data collection, and documentation. The role also involves working closely with the research team and ensuring compliance with ethical standards and regulatory requirements.

 

Qualifications

 

  • Informed Consent and Protocol experience
  • Proficiency in clinical research practices
  • Previous experience with clinical trials
  • Strong organizational and time management skills
  • Excellent attention to detail
  • Good communication and interpersonal skills
  • Ability to work effectively in a team
  • Experience in data collection and documentation
  • Bachelor's degree in a related field (e.g., Life Sciences, Pharmacy, Nursing)
  • Knowledge of regulatory requirements for clinical research