Job Title: R&D Microbiologist Experience Level: 0-1 year. Location: Siruseri, Chennai About Us MicroGo is committed to the One Health approach, integrating human, animal, and environmental health. Their work culture is characterized by openness, interactivity, and a non-hierarchical structure. Role Summary They are seeking a skilled and motivated microbiologist to join their team. The chosen person will take care of the microbiology lab according to USP-1117 standards, perform tests on microbes, and help with farming projects that focus on minimizing losses after harvest. This role involves collaborating with farmers, agricultural experts, and government entities to pilot and field-test new storage technologies. Key Responsibilities - Maintain and operate the microbiological laboratory in compliance with USP-1117 standards for research and quality control. -Conduct microbial examination, culturing, identification, media preparation, and aut...
medONE Pharma Solutions
Requires Clinical Process Associate
medONE is seeking a motivated and detail-oriented Clinical Process Associate to contribute to the success of company's clinical trials. If you're passionate about advancing medical research and thrive in a fast-paced environment, and want to hear from you!
As a Clinical Process Associate, you will play a crucial role in supporting the efficient and accurate execution of clinical trials.
You will be responsible for a variety of administrative and operational tasks, ensuring compliance with regulatory guidelines and internal SOPs.
Responsibilities:
-Assist with the preparation, review, and maintenance of clinical trial documentation (e.g., study protocols, informed consent forms, regulatory submissions).
- Maintain and update clinical trial databases and tracking systems.
-Coordinate and track the shipment and receipt of clinical trial supplies.
-Assist with the scheduling and coordination of site visits and meetings.
-Support the preparation of study-related reports and presentations.
-Ensure adherence to Good Clinical Practice (GCP) guidelines and company SOPs..
-Communicate effectively with internal and external stakeholders.
-Assist with the management of Investigator Site Files (ISFs) and Trial Master Files (TMFs).
-Assist with the preparation of audit and inspection readiness activities.
Qualifications:
-Bachelor's degree in a life science or related field.
-Minimum of 1 year of experience in a clinical research setting.
-Strong understanding of GCP guidelines and regulatory requirements.
-Excellent organizational and time management skills.
-Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
-Strong attention to detail and accuracy.
-Excellent communication and interpersonal skills.
-Ability to work independently and as part of a team.
-Experience with electronic data capture (EDC) systems (preferred).
Benefits:
-Opportunities for professional growth and development.
-Collaborative and supportive work environment.
-Chance to contribute to cutting-edge medical research.
Mail your resumes to: rashioffice54@gmail.com/jobs@moplindia.com
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