Department of Virology Post Graduate Institute of Medical Education & Research, Sector 12A, Chandigarh-160012 NOMPS/ANRF/25/27 Date: 02/08/2025 Recruitment Notice Applications are invited from eligible candidates for an Extramural (funded by DST-ANRF; Project ID: CRG/2023/007689) research project entitled "Nevel neurovascular organoids to understand the neuropathogenesis of non-polio enterovirus" at Department of Virology at PGIMER, Chandigarh on a tenure basis. The following post will be filled up on a purely contractual basis. 1. Sr No.: 1 2. Name of the Post:Junior Research Fellow 3. No. Of Post : 01 4. Qualification: Essential qualification: a) Masters in a Virology/Microbiology Biotechnology/Brochemistry/Life Sciences / Genetics from recognised institution with first class aggregate b) Scholars who are selected through eligibility Tests-CSIR-UGC NET, (including national Cat-1, II and III), GATE or any National level examination conducted by Central...
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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