203 Research Associate Jobs - Page 9

Sr Medical Research Associate POSITION PURPOSE: Senior Medical Research Associate is key resource personnel in Medical Affairs for managing and executing Phase IV studies (including Post marketing surveillance studies, Non-interventional studies (NIS), mandated Phase IV studies including interventional post-approval trials) activities across all business areas. He/She is responsible for all operational and quality aspects of the allocated studies in compliance with ICH-GCP, local regulations and within the agreed timelines and cost. YOUR TASKS AND RESPONSIBILITIES: As Individual contributor: To Coordinate all study activities like CRO selection, preparation of study documents for review, site selection and feasibility, update relevant tracking systems on an on-ging basis, implement quality checks especially for outsourced studies and manage clinical trial oversight, manage study budget and required resources, site monitoring, quality review and archival. The major responsibility includes on-time and on-budget completions in India. To have an oversight on CRO partners for outsourced studies by conducting oversight quality visits at sites if applicable, conduct regular meetings and seek regular updates on study progress. Organize Investigators meetings if applicable, conduct site feasibility visits and site initiation visits if applicable to ensure that the study staff are well trained and familiar with the protocol and study procedures. Responsible for the implementation and training of standardized processes within the study and according to organizational SOPs. Development of essential studies as per the local requirement and creating the essential documents like protocol, ICF etc with coordination with global/local team members. Ensures that essential documents meet the quality expectations of regulatory requirements in India and Bayer guidelines/SOPs. Reports and/or communication with Health Authority/IRB/Investigators and global/country study team, marketing/sales departments to update and share study progress, protocol, safety and other issues where necessary and submit annual-bi-annual report to regulatory teams in order to meet local requirements. To provide efficient and timely study updates to Manager Medical Operations. WHO YOU ARE: A Qualified pharmacy or science/life-science graduate/ postgraduate. Desirable previous experience of around 5 years in clinical research. Strong skills in managing stakeholders and good understanding of handling clinical trials in line with ICH-GCP and local regulations. Business Acumen displaying ability to operate cross-functionally Persistent in approach, drives objectives despite setbacks AdEopts an optimistic outlook Collaborates effectively, team player, team leader Inquisitive mindset, challenges status quo, proactive in approach.

(a) A graduate degree in law with a minimum aggregate of 55% marks from any Institution, recognised by the Bar Council of India; (b) Minimum experience of two years as an Advocate/ Research Associate/ Legal Assistant in a Court of Law or any Government Office or reputed Law Firm or in an office of a reputed Advocate; and (c) Should have passed the All India Bar Examination (AIBE). Desirable qualifications (a) Post Graduate degree in law; (b) Research and analytical skills, writing abilities, including retrieval of desired information from various search engines/ processes such as eSCR, Manupatra, SCC Online, LexisNexis, Westlaw. etc; and (c) Must have good knowledge of the operation of computers and skills of using common software like MS Office, etc. Disqualifications (a) Must not be engaged, or appointed elsewhere on an honorarium payment basis or otherwise; (b) Should not have been involved in any criminal case, whether convicted or against whom a criminal investigation is ongoing or be named as an accused in an FIR; (c) Must not be facing any disciplinary proceeding before the Bar Council of India, Bar Council of any State or Institutes or any other authority.

Project Technical Support III - ICMR MINDS Project Division Non Division User Contact Person Ms. Lincy Thomas Job Details Brief Description about the Project To develop and implement a service delivery model that would result in high coverage (at least 70%) of screening, linkage to care, and management of priority mental disorders among persons seeking care for NCDs at public health facilities. To assess the feasibility of adopting the implementation model by the health care system. To determine the cost of the implementation of the service delivery model. Methods: It will be a multi-site, quasi-experimental, within-site, interrupted time series design implementation study using a mixed-methods design incorporating formative and evaluative components into iterative improvement cycles. The implementation model consisting of screening, linkage, and treatment in mental health services integrating into NCD care, will be optimized with Consolidated Framework for Implementation Research (CFIR) while implementing the model in at least three blocks of seven districts of seven states. Expected outcome: Increase in the proportion of patients screened and managed for mental health disorders among those screened positive for or having established NCDs. Project Technical Support - III No.of Vacancy: One Prefered Qualifications: Three Years Graduate in relevant subject/field/Social worker/Psychologist + three years experience or PG in relevant subject/field Experience : Minimum of 1 year of fieldwork in rural areas of Karnataka Age Limit: 35 years Language : Kannada, English, Telugu, Tamil, Hindi Salary : Rs.36,400/- per month Location : Bengaluru rural and urban areas Roles and Responsibilities: Project Technical Support- III shall assist PI and Co-PI with all mental health and behavioral aspects of the study. They will coordinate activities in each of the healthcare facilities designated to them. They will provide training to the junior staff capturing data and ensuring fidelity to the intervention protocol. They will coordinate with the project manager in tracking the participants who are referred to the HWC. will undergo training in the field application of various study questionnaires and clinical measures including pilot testing of these questionnaires. They will administer various tablet-based questionnaires and clinical measures to participants in the study. They will conduct all interviews under the daily supervision of the Project Manager and Research Associate. The assessment staff members will provide feedback to the Project Research Scientist during daily check-ins and weekly team meetings regarding any project-related issues. Interested candidates may send their Resume to: The Principal Investigatior