Ph.D. Training Program Institute of Bioinformatics (IOB) is inviting applications for Junior Research Fellow (JRF) in a Project-based position. The selected candidate will work on a project titled "Epigenetic Basis of Cancer Progression and Therapy Resistance". About Institute of Bioinformatics Institute of Bioinformatics (IOB) is an internationally renowned interdisciplinary research institution founded in 2002 by Akhilesh Pandey, M.D. Ph.D. in 2002. IOB is a Manipal Academy of Higher Education (MAHE) recognized research center. IOB has obtained several grants including Center of Excellence from key funding bodies including DBT/Wellcome Trust India Alliance (Center for Rare Disease Diagnosis, Research, and Training), DBT, DST and ICMR. IOB has a strong track-record in training interdisciplinary scientists through its Ph.D. program with 67 students who have graduated, many of whom are current postdoctoral fellows, staff or faculty in internationally renowned ins...
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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