• 541
  • Active Jobs Found
    (Last Updated: Jan 29, 2023)
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  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023

Responsibilities Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out. Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan. Developing effective relationships with investigator site staff to ensure that key clinical metrics are met. Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues. Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines. You will be operating as a key part of a global study team and plays a fundamental role in our clients’ drug development processes.   Qualification & Experience 4+ years of Onsite monitoring experience in phase I-III trials as a CRA 2+ years of Global project experience in Oncology studies. College degree in medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication Ability to work to tight deadlines Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license  

  • clinical research
  • pharmacovigilance
  • mbbs

Executive - Nutrition

Samyog Health Foods (Prolicious)

Full time
  • 1+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023
  • 1+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023

Responsibilities Engage in a long-term association with other nutritionists and healthcare professionals for collaboration, education about the product and product development feedback. Engage with different target groups for nutrition-based outreach programs. Co-ordinate with R & D team regarding the nutritional requirements for product development. Co-ordinate with marketing team for product promotions and content development for claims and communications Leverage nutrition knowledge for product promotion in form of scientific information for various presentations.   Qualification & Experience M.Sc. in Food Nutrition & Dietetics OR P.G. diploma in Dietetics /M. Sc in Sports Nutrition 1-4 years of experience Comfortable for field based / travelling profile Good written and oral communication skills. Good interpersonal skills and ability to work in team. Skilled in MS office (excel, power-point)  

  • Quality control
  • mbbs
  • MD

Nurse

Dr Sunny Medical Centre

Full time
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023

Responsibilities The staff nurse will be responsible for patient assessment, as well as planning of care and subsequent recovery. Provides professional nursing services and patient care in variety of inpatient and outpatient settings. Follows established nursing process, including patient assessment, nursing diagnosis, planning, intervention, and evaluation. Ensures adherence to hospital or department and university policies, and nursing procedures, standards, and practices.   Qualification & Experience Graduate of a nationally accredited Nursing program 1-5 Years of experience after Registration Freshers can also apply Certification/State registration (KNC or any other state) Knowledge of patient evaluation and triage procedures. Knowledge of clinical operations and procedures. Knowledge of nursing theory and practice. Ability to plan, implement, and evaluate individual patient care programs. Skill in preparing and maintaining patient records. Knowledge of clinical and/or surgical facilities, instruments, and equipment. Knowledge of appropriate procedures and standards for the administration of medications and patient care aids.  

  • clinical research
  • Operations
  • hospital management
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 24, 2023
  • End Date: Mar 24, 2023

Qualification & Experience MD, DNB, MEM, FEM, MRCEM Fresher's and Experienced both can apply  

  • mbbs
  • MD
  • Operations

Clinical Data Manager

Eli Lilly and Company

Full time
  • 3+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 3+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Responsibilities Execute Lilly business requirements for the study/program for vendors to deliver clinical trial data Ensure that data management deliverables are delivered to scope, cost, and time objectives Coordinate end-to-end data management activities – from study set up through trial execution through dataset delivery, including on time delivery of a quality, locked database Ensure flow of data, including across niche vendors and niche data sources (pharmacokinetic, immunogenicity, biomarker) Contribute to key deliverables (i.e. Data Management Plan, Project Plan, database, and observed datasets) Participate in submission, inspection and regulatory response activities Central coding activities completed Archiving and decommissioning of study related data management documents and content Ensure that data acquisition, database design, data validation, data review, central coding and observed dataset requirements are reflective of specific protocol objectives Adhere to standards decisions, implementation and compliance for the study/program Track and report out key study build, execution and data deliverable metrics Help create scope scenarios and negotiate outcomes with study teams while considering the cost and value Facilitate the integration of disparate data sources into datasets for decision making Utilize therapeutic knowledge and possess a deep understanding of the technology used to review data to ensure database deliverables are consistent and accurate Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to data deliverables Continually seek and implement means of improving processes to reduce cycle time and decrease work effort Represent Data and Analytics processes in cross-functional initiatives Actively participate in shared learning across Data and Analytics organization   Qualification & Experience 3 years Data Management experience or 5 years experience in drug development in areas intersecting with clinical data management (e.g., clinical operations, statistics, information technology, health outcomes, etc.) Masters degree in medical field, Informatics, Life Sciences, Health Information Administration, Statistics, Information Technology, Nursing, Pharmacy, Business  

  • pharma
  • clinical research
  • pharmacovigilance

Analyst-Clinical Data Management

Accenture

Full time
  • 3+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 3+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Responsibilities In this role, you are required to analyze and solve lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors You may have limited exposure with clients and/or Accenture management You will be given moderate level instructions on daily work tasks and detailed instructions on new assignments You will need to be well versed with basic statistics and terms involved in the day to day business and use it while discussing with stakeholders You will be expected to constantly be on the lookout for ways to enhance value for your respective stakeholders/clients The decisions you make impact your work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work.   Qualification & Experience Any Graduation 3 to 5 years of experience  

  • pharma
  • clinical research
  • pharmacovigilance

Pharmacovigilance Associate I

Teva Pharmaceuticals

Full time
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 0-1 years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Responsibilities Processing adverse events reports from post marketing sources into Teva's global safety database: The different sources / types of reports includes:Reports from the scientific literature, Teva partners (other pharmaceutical companies), Health Authorities, Non-interventional studies and other programs The processing includes Adverse Events coding (in medical dictionary - MedDRA), drug coding in the Company Product Dictionary, seriousness and labeling assessment and submission to health authorities Working in global environment: Interacting with other global PhV units and local PhV reps. around the world Taking part in the development and maintenance of an efficient and robust Pharmacovigilance system.   Qualifications B.Pharma / M.Pharma / Bsc / Msc  

  • pharma
  • pharmacovigilance
  • bpharm

IPQC Incharge

Natural Capsules Limited

Full time
  • 4+ years
  • Not Disclosed
  • Puducherry, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 4+ years
  • Not Disclosed
  • Puducherry, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Responsibilities This position reports to GM – CQA Monitoring and enforcing completion of activities of IPQA, FQA, Packing QA and Process QA. For assisting audit preparations – Customer audits, Regulatory audits or any other by any certification agency. Enforcing legible online documentation of BMR, logbook and its enclosures. Responsible for enforcing use of rejection mechanisms on the Machines, Responsible for Pre-dispatch audits (Quality & Logistics) Responsible for Finished Product Batch release   Qualification & Experience BSC Chemistry with 4-5 years of experience in Quality Assurance Candidate should be 30-35 years of age  

  • Quality control
  • pharmacovigilance
  • Drug Safety

Project Manager / Research Scientist

Athenese-Dx

Full time
  • 2+ years
  • Not Disclosed
  • Chennai, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 2+ years
  • Not Disclosed
  • Chennai, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

They are hiring Project Manager / Research Scientist FLUORESCENT IMMUNOASSAY / RAPID TEST   Qualification & Experience MSC / M Tech in Life Science 2 to 5 years in IVD Industries  

  • Quality control
  • clinical research
  • pharmacovigilance

Senior Executive - Clinical Research Associate

Sun Pharmaceutical Industries Ltd.

Full time
  • 4+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Feb 23, 2023
  • 4+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Feb 23, 2023

Responsibilities Identification of potential sites for studies. Coordination with Clinical sites, vendors and internal stakeholders. Conducting site assessment through feasibility and site qualification visit. Provide training and guidance to sites throughout the study. Perform monitoring visits at participating sites and review data and ensure compliance and subject safety and wellbeing. Preparing the report, supporting the PM in drafting the plans, collection of information, adherence to study timelines   Qualification & Experience M.Pharm, / MSc 4 years experience in related field Computers, proficiency in word and excel, exp. Of working with clinical trial systems like ctms, edc, etc.  

  • pharma
  • clinical research
  • pharmacovigilance

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