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  • Join PAREXEL as Regulatory Affairs Associate

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.

    Post : Regulatory Affairs Associate

  • More than 30,000 Takeda employees working in more than 70 countries are committed to improving quality of life for patients, who remain at the center of everything we do. Takeda Pharmaceutical Company Limited is a global, research and development-driven organization working internally and with external partners to translate science into life-changing medicines. Takeda focuses on the core therapeutic areas of oncology, gastroenterology, neuroscience and providing vaccines that address the most important infectious diseases. Novel products, especially in oncology and gastroenterology, as well as our presence in emerging markets, fuel our growth.

    Post : Senior Clinical Research Associate

    Job Description
    Objectives
    Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and Takeda requirements 

    Accountabilities :  
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with study protocol and applicable regulatory requirements
    • Work with CROs to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
    • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
    • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
    • Ensure site documents are available for filing in the Trial Master File (TMF) and verify that documents are maintained in accordance with GCP and local regulatory requirements
    • Ensure 100% adherence to monitoring and study plan
    • Support clinical quality in managing CAPAs and other study audit observations
    • Support Clinical Operations Lead/ Clinical Operations Manager in performing CRO oversight as per agreed parameters
    • Ensures adherence to study budget through constant monitoring for allocated study(ies)
    • Ensures dissemination of study updates to relevant stakeholders as per agreed timelines

    Candidate Profile
    • Master’s or Ph. D degree in scientific discipline or healthcare with >5 years’ experience in clinical trials industry as Clinical Research Associate
    • Good working knowledge of GCP and local clinical trial rules and regulations
    • Organizational and problem-solving skills
    • Superior communication, strategic, interpersonal, and negotiating skill
    • Proven/ stable performance records over past 2-3 years

    Additional Information
    Experience : >5 years
    Qualification : Master’s or Ph. D degree in scientific discipline or healthcare
    Location : Mumbai, Maharashtra
    Industry Type : Pharma/ Healthcare/ Clinical research
    Functional Area : Research & Development
    End Date : 20th May 2024

    Apply Online

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  • Work as Senior Clinical Scientist at Bristol Myers Squibb

    Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions.

  • Teva Pharmaceutical looking for Regulatory Affairs Associate

    Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.

    Post : Regulatory Affairs Associate I

  • MSD looking for Specialist Quality

    Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

    Post : Specialist Quality

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Multiple Department at Sun Pharma - Only for Female

    Sun Pharmaceutical Industries Limited is taking this opportunity to balance employment and the medications to the world. We arc hereby inviting candidates who are interested to join India's No. I company in Pharmaceutical sector.

    Manufacturing / Packing (Parenteral)
    Post : Technician to Senior Executive
    Experience : 2-8 Years
    Qualification : ITI/ Diploma/B.Pharma / M.Pharma

  • Indegene looking for Scientific Writing Lead

    We help biopharmaceutical, emerging biotech and medical device companies develop products, get them to the market, and grow their impact through the life cycle in a more effective, efficient, and modern way. We bring together healthcare domain expertise, fit-for-purpose technology, and an agile operating model to provide a diverse range of solutions. These aim to deliver, amongst other outcomes, a personalized, scalable and omnichannel experience for patients and physicians.

  • Indoco Remedies Walk In Drive for M.Pharm, B.Pharm, MSc in Quality Control, Production

    Indoco Remedies Ltd., is a fully integrated, research-oriented pharma company engaged in the manufacturing and marketing of Formulations and Active Pharmaceutical Ingredients (APIs). We have seven decades of presence in the Indian Pharma market and a strong foothold in the international market across 55 countries. Indoco, a USD 166 million company, employs around 6000 personnel, including over 300 skilled scientists.

    WALK-IN-INTERVIEW For our tablet manufacturing facility in Goa

  • Interview for M.Pharm, B.Pharm, M.Sc in Production, QA, QC, Microbiology at Emcure

    Emcure is fast-growing Indian pharmaceutical company engaged in developing, manufacturing, and marketing a broad range of pharmaceutical products globally. With a presence in over 70 countries, Emcure's goal is to constantly innovate and deliver affordable & high-quality healthcare solutions to people.

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Production, QC, QA at Aarti Pharmalabs

    Aarti Pharmalabs Limited engages in the development of Active Pharmaceutical Ingredients (API) and New Chemical Entities (NCE), API intermediates, Regulatory Starting Materials (RSM), Basic Starting Materials, Key Building Blocks, and Xanthine Derivatives for use in clinical testing and commercial production. In addition to process R&D, we provide stability studies, scale-up and process optimisation, process validations, and commercial manufacturing.

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