For the position of Clinical Research Coordinator (CRC), we are seeking a highly driven and meticulous new hire to join our team. This position presents a fantastic chance to begin a career in clinical research and advance within our company. As a CRC, managing clinical trials and making sure regulations are followed are your responsibilities.
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Responsibilities
- Help with the planning, execution, and closing of studies.
- Organize the enrollment, retention, and recruitment of patients.
- Handle research data management, including query resolution and data entry.
- Keep current and accurate study records.
- Make ensuring that company rules, legal obligations, and good clinical practice (GCP) are all followed.
- Work together with cross-functional teams made up of sponsors, monitors, and investigators.
- Create and carry out plans and processes particular to the study.
Requirements:
- B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
- 0–1 year of clinical research experience (newcomers are welcome to apply).
- a basic understanding of clinical research principles, regulatory restrictions, and GCP.
- outstanding problem-solving, organizing, and communication abilities.
- the capacity to prioritize work and function well in a collaborative setting.
Training Provided:
- thorough instruction on corporate policies, legal obligations, and GCP.
- mentoring and training by seasoned CRCs while working on the job.
- Opportunities in the field of clinical research for professional development and advancement.
How To Apply
Please send your resume and cover letter to innovationclinicalresearch19@gmail.com if you’re interested in this opportunity.
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