1.0 - 5.0 years

0 Lacs

hyderabad, telangana

On-site

You will be playing a key role in developing clinical database products across various therapeutic areas such as Metabolic & CV, Neuroscience, Autoimmune, Oncology, and Respiratory with a focus on high quality to support Meta-analysis. Your responsibilities will include analyzing and annotating trial design information, treatments, demographics, and outcomes data from clinical literature sources. You will also be required to digitize results from graphs accurately and consistently. Collaboration will be a key aspect of your role as you work with lead consultants, peer data analysts, and quality managers to contribute to database rules, specifications, and quality processes. Additionally, you will undergo relevant training programs in areas such as Statistics, R coding, Systematic Literature review, and Data analysis methods to enhance your skills and advance within the organization. To qualify for this position, you should have a Master's degree in Pharmacology or Pharmaceutics (with relevant experience), PharmaD, Clinical Practice, Master's in Public Health, or Epidemiology. A minimum of 1-2 years of experience in Information science, Systematic Literature review, Health-economics, or public health sectors is required, with preference given to those with pharmaceutical industry experience. Strong knowledge of Pharmacology, clinical research, and clinical development processes is essential, along with familiarity with trial designs, Pharma Industry data standards, and ontologies. Having skills in statistics, data management tools like R, and a willingness to learn and collaborate in a team environment are crucial for success in this role. Excellent interpersonal skills, strong learning abilities, and a passion for supporting databases in various disease areas will be valuable assets that you bring to the team.,

Posted 4 days ago

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Centralized Monitoring Assistant IQVIA

1 - 3 years

1 - 3 Lacs

Kochi

Work from Office

Role : Centralized Monitoring Assistant Skill : Must have Good Clinical Practices (GCP) Mode : Hybrid (3 Days Work from Kochi office & 2 days from HOME) Experience : 0.6 Month to max 3 years of Exp Only. Job Location : Kochi and Ahmedabad Educational Qualification: Graduate/Post Graduate in Life Sciences PURPOSE • Engage in company training program to gain knowledge and skills required to provide administrative support to • projects in accordance with SOPs, policies, good clinical practices, and applicable regulatory requirements. • Meeting quality and timeline metrics under direction of line manager and/or other designated team members RESPONSIBILITIES Complete appropriate role-specific training to perform job duties. Under supervision, perform assigned administrative tasks to support team members with project execution • (examples of such tasks include but not limited to running system reports, preparing and distributing status • reports, creating and maintaining study documents, etc.). Under supervision, assist in updating and maintaining systems within project timelines/plans. Perform the activities as per the task list delegated by Centralized Monitoring Specialist/Centralized Monitoring Lead. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Basic knowledge of applicable research and regulatory requirements, i.e., ICH GCP and relevant local laws, regulations, and guidelines. Exposure to MS Applications including but not limited to Microsoft Word, Excel and PowerPoint. Effective written and verbal communication skills including good command of English language. Effective time management skills. Results and detail-oriented approach to work delivery and output. Ability to establish and maintain effective working relationships with coworkers, managers and clients Strong listening and phone skills. Good data entry skills.

Posted 3 months ago

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