Vimta Labs Ltd. is a leading contract research and testing organization providing a wide range of services in clinical research, environmental testing, pharmaceutical analysis, and food testing. With state-of-the-art facilities and a commitment to quality, Vimta Labs ensures excellence in compliance with global regulatory standards. The company is now hiring Medical Investigators (Male) for its Cherlapally facility in Hyderabad.
Job Responsibilities
The Medical Investigator will report to the Principal Investigator and play a crucial role in ensuring the adherence to Good Clinical Practices (GCP) in clinical research studies. Key responsibilities include:
Primary Responsibilities:
- Ensuring compliance with Good Clinical Practices (GCP) and standard operating procedures (SOPs).
- Conducting planned clinical studies as per protocol requirements.
- Reviewing pre-study health records of volunteers.
- Obtaining written informed consent before volunteer participation.
- Ensuring clinical data is complete, accurate, and recorded as per protocol and SOPs.
- Assessing and documenting UDS reports & additional test reports.
- Documenting volunteer eligibility status.
- Monitoring daily temperature logs, emergency medication kits, and expired medication disposal.
- Conducting group briefings on Informed Consent Forms (ICF).
- Managing Adverse Events (AE) and Serious Adverse Events (SAE), including reporting and documentation.
- Monitoring trial progress and data consistency.
- Overseeing ICU maintenance and emergency condition management.
- Supervising vital signs monitoring, ECG, phlebotomy, and X-ray procedures.
- Ensuring the verification and safe disposal of X-ray films and reports.
- Conducting post-study report assessments and documentation.
- Ensuring Case Report Forms (CRFs) completion and documentation.
Secondary Responsibilities:
- Reviewing Informed Consent Forms (ICFs) and Case Report Forms (CRFs).
- Screening and evaluating volunteers for study participation.
- Monitoring drug administration to volunteers.
Qualification & Requirements
- MBBS degree is mandatory.
- Medical Registration is required.
- Experience: 1 to 3 years in the Clinical Research industry.
- Male candidates only (as the position includes night shifts).
- Strong understanding of clinical research protocols and GCP guidelines.
- Experience in AE and SAE management, clinical trials monitoring, and volunteer screening.
- Ability to handle emergency conditions and maintain ICU procedures.
Skills Required
- Knowledge of Good Clinical Practices (GCP) and clinical research methodologies.
- Strong documentation and reporting skills.
- Attention to detail in data verification and compliance.
- Ability to work night shifts and in a fast-paced clinical research environment.
- Excellent teamwork and communication skills.
How to Apply
Interested candidates who meet the above qualifications can apply by sending their updated resumes to keerthana.rojanala@vimta.com.
