Skip to main content
Upload your CV and find your next job on Indeed!

Biomedical Trainee jobs

Sort by: -

People also searched:

bio medical engineer hospital

Job Post Details

Trainee Clinical Research - job post

WorkSure
Delhi, Delhi
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Shift and schedule

  • Day shift

Location

Delhi, Delhi

Full job description

Requirements:

  • Educational Qualification:Sc, MSc, D.Pharm , B Pharm, M Pharm, Biotechnology, Microbiology and any other degree in life sciences candidates can apply.
  • Strong interest in clinical research and a desire to learn and develop within the field.
  • Good organizational skills and attention to detail.
  • Excellent interpersonal and communication skills
  • Ability to work effectively both independently and as part of a team
  • Flexibility to adapt to changing priorities and responsibilities.
  • Candidates with experience will have a preference

Job Description:

  • Strong Knowledge of ICH-GCP E6 R2 guidelines and other Indian and international regulatory guidelines
  • To facilitate and coordinate the all daily clinical research trial activities, for assigned projects
  • Support in managing study visits, following study protocols and guidelines.
  • Help with logistics such as ordering and maintaining supplies needed for the study
  • Assist in maintaining study-related documentation, conduct reminder calls, manage study subject’s reimbursements, AE & SAE reporting, Source Document Maintenance
  • Assist in Investigator Site File management, IP accountability & CRF Completion, completion of all study logs
  • Working with the monitors (CRA’s) during their monitoring visits and participate in data verification, source document verification (SDV), and quality control activities.
  • Maintain effective communication with study team members, investigators, and study participants
  • Attend study team meetings, providing updates on study progress and challenges.
  • Ensure adherence to regulatory requirements and guidelines throughout the study.
  • Assist in maintaining accurate and up-to-date regulatory documents
  • Stay informed about industry trends and advancements in clinical research.

Job Type: Full Time/Day shift (3-6 months on-site training)

Salary: Stipend as per industry norms

Let Employers Find YouUpload Your Resume