WhatsAppMessage Now LinkedInConnect Now CallCall Now WhatsAppJoin Group

Clinoxy

Menu
Register Now

Your Trusted Partner for Skilled Resource Supply

At clinOXY, we offer a diverse pool of meticulously trained resources equipped with industry-relevant skills and knowledge. Our Students are trained in Clinical Research, Pharmacovigilance, Clinical Data Management, Regulatory Affairs, Medical Writing, Medical Devices & IVD, Medical Coding, Medical Communications, Health Informatics and Bioinformatics. Our trained resources bring a distinct advantage to your projects, delivering efficiency, reliability and excellence in every task.

 

At clinOXY, we offer Practical Oriented Trainings enriched with Real-Time Experiences. Upon completion of our training programs, our students gain proficiency in various areas and can undertake the following tasks:

  • Write Protocols, Informed Consent Forms (ICF), Clinical Study Reports (CSR), and other essential clinical trial documents.
  • Directly engage in clinical trial site activities with minimal onboarding training.
  • Assume roles such as Clinical Research Coordinator and Clinical Research Associate with confidence.
  • Adhere to Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP) guidelines.
  • Conduct randomization and blinding activities with precision.
  • Perform feasibility analysis for clinical trials.
  • Handle Case Processing activities in Pharmacovigilance, including Triage, Duplicate Check, Case Registration, Query Management, and Case Narratives.
  • Utilize Safety Databases like ARGUS in Pharmacovigilance and Clinical Databases like Inform ORACLE in Clinical Data Management.
  • Execute Clinical Trial Case Processing, Post-Marketing Case Processing, and Literature Case Processing proficiently.
  • Manage Study Start-Up, Study Conduct, and Study Close-Out activities in Clinical Data Management.
  • Draft Data Validation Plans (DVP) effectively.
  • Conduct Validation activities in Clinical Data Management, including Discrepancy Management, Query Management, Serious Adverse Event (SAE) Reconciliation, and Laboratory Reconciliation.
  • Engage in Regulatory Documentation, including Pre and Post-approval documents, Filings, Investigational New Drug (IND), New Drug Application (NDA), Abbreviated New Drug Application (ANDA), and Biologics License Application (BLA).
  • Prepare eCTD submissions proficiently.
  • Write Medical Writing documents such as Protocols, Informed Consent Forms, Investigator Brochures, Clinical Study Reports, and Case Safety Reports.
  • Conduct Literature Screening effectively using PubMed and EMBASE.
  • Write Disease Write-Ups, Medical Communications, Content for Healthcare Websites, and Drug Information.
  • Demonstrate good knowledge of Medical Devices, particularly in EU-MDR, EU-IVDR, and IMDR.
  • Prepare Medical Device Regulatory Documents such as Instruction for Use (IFU), Direction for Use (DFU), Surgical Procedures, Technical Documents, Design History File (DHF), Risk Evaluations, Post-Marketing Clinical Follow-Ups (PMCF), Clinical Evaluation Plans (CEP), and Clinical Evaluation Reports (CER).

We ensure that our students receive comprehensive training, enabling them to excel in various roles within the Clinical Research, Pharmacovigilance, Clinical Data Management, Regulatory Affairs, Medical Writing, Medical Devices & IVD, Medical Coding, Medical Communications, Health Informatics and Bioinformatics.

In our comprehensive training programs, we empower Fresher candidates to emerge as seasoned Professionals ready to excel in corporate environments. We cover the following crucial aspects:

  • Smooth Onboarding Processes: Mastering the onboarding formalities essential for seamless integration into corporate settings.
  • Significance of Onboarding Trainings: Understanding the pivotal role of onboarding programs in navigating corporate culture and expectations.
  • Effective Interpersonal Communication: Learning to engage and collaborate with diverse colleagues within the organization.
  • Strategic Team Communication: Fostering excellent communication channels within teams to enhance productivity and synergy.
  • Task Prioritization and Timely Deliveries: Developing skills to prioritize daily tasks and ensure timely submissions, crucial for meeting corporate deadlines.
  • Efficient Meeting Management: Techniques for organizing both internal and external meetings with precision and efficacy.
  • Proficient MOM Preparation: Mastery in crafting effective Minutes of Meeting (MOM) to document discussions and action points.
  • Compliance with POSH Act: Understanding and adhering to the Sexual Harassment of Women at Workplace (Prevention, Prohibition, and Redressal) Act, 2013, to promote a safe and inclusive work environment.
  • Embracing First Time Quality: Cultivating a mindset focused on delivering top-notch quality work from the outset.
  • Adherence to Code of Conduct: Upholding corporate standards and ethics outlined in the company's Code of Conduct.
  • Anti-Bribery and Anti-Corruption Policies: Familiarity with policies and procedures to combat bribery and corruption, essential for maintaining corporate integrity.
  • Enhanced Problem-Solving, Communication, and Ethical Skills: Developing critical skills for navigating complex corporate challenges with integrity and professionalism.
  • Cultivating Adaptability, Time Management, and Teamwork: Embracing adaptability, effective time management, and collaborative teamwork as cornerstones of corporate success.

Our training equips candidates with the requisite knowledge and skills to thrive in dynamic corporate environments, ensuring they become valuable assets to their organizations from day one.

Enquire Now
Register Now