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Clinical courses


Clinical courses

  • Require Senior Research Scientist at Reliance Life Sciences

    Reliance Life Sciences is a medical biotechnology-led company engaged in research and development, manufacturing and marketing of differentiated medical products and services, used to treat patients primarily in intensive and critical care units in hospitals. Three core businesses of RLS are plasma proteins, biosimilars, and later generation oncology pharmaceuticals. In addition, it has initiatives in clinical research, molecular medicine, regenerative medicine, genetherapy, peptides and oligonucleotides.

  • 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
    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.

  • Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.

    Post : Associate I – Regulatory Conformance

    Job Description 
    As an associate, your focus on the job will contribute in achieving your team’s tasks and goals. This is a multifaceted role that will offer you a number of opportunities to enhance your skills. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.  It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

    Job Description
    • Committed to quality and excellence in compliance and conformance
    • With the reasonable understanding of regional regulations, would perform the evaluation of the notifications assigned.
    • Accountable for maintaining the HA status in corporate change and dossier management system for the allocated Regions / Markets
    • Contributes independently and manages own time to meet the timelines.
    • Work in collaboration with GRA colleagues to ensure the gaps are identified and escalated on time.
    • Independently Perform accurate updates in system for most of the cases and consult with TL/Designee for clarification of any discrepancies in complex cases, before updating the system.
    • Makes informed decisions on straight cases within guidelines and policies
    • Support for updates in system for License withdrawals
    • Operate in line with internal SOPs and policies
    • Adhere to standard turnaround timelines
    • Escalate any potential compliance issues to management
    • Support periodic and ad-hoc system reports to estimate metrics
    • Contribute to local and regional regulatory initiatives promoting a culture aligned with Pfizer values
    • Assist in ensuring internal regulatory processes and procedures are well documented
    • Assist in remediation activities
    • Support the teams in ADHOC activities
    • Shares the learning time to time with the team colleagues

    Technical Skills
    • Theorotical Knowledge on Regulatory Affairs / Compliance
    • Experienced in Regulatory / Quality Assurance/ Production or any other functions in Pharmaceutical or related industries
    • Diligence and attention to detail
    • Good communication skills
    • Understanding stakeholder needs
    Behavioral/Any other Skills – An assertive, results oriented, positive “can do” attitude, and Time management skills. Preferred

    Candidate Profile
    Qualification – Master’s / Bachelor’s degree or equivalent i.e. degree in Chemistry, Pharmacy, or a related life sciences.  Preferred Year Of Experience - 2 to 4 years of experience 
    Type of Experience – Any relevant experience in Pharmaceutical or relevant industry. Experience in Regulatory or Quality or Compliance roles is preferable.

    Additional Information
    Experience : 2 to 4 years
    Qualification : Master’s / Bachelor’s degree or equivalent
    Location : Chennai
    Industry Type : Pharma/ Healthcare/ Clinical research
    Functional Area : Regulatory
    End Date : 20th May 2024

    Apply Online

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  • 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

  • Biotechnology Industry Research Assistance Council Hiring Associate Consultant - MSc in Pharma, Life Sciences Apply

    Biotechnology Industry Research Assistance Council (BIRAC) is a not-for-profit Section 8, Schedule B, Public Sector Enterprise, under Department of Biotechnology (DBT), Government of India as an Interface Agency to strengthen and empower the emerging Biotech enterprise to undertake strategic research and innovation, addressing nationally relevant product development needs.

  • Applications are invited for post of Project Associate at IIIM

    The Laboratory was established in 1941 as a research and production centre, known as Drug Research Laboratory of J&K State and was later taken over by Council of Scientific & Industrial Research (CSIR) of Govt. of India in December 1957 as Regional Research Laboratory, Jammu. In view of its core strength in natural products based drug discovery, the mandate of Institute was redefined in 2005 and its name changed to Indian Institute of Integrative Medicine (IIIM).

  • Applicants are invited for post of Research Associate at National Institute for Plant Biotechnology

    The institute was founded in 1985 as the ‘Biotechnology Centre’ of Indian Agricultural Research Institute (IARI) for molecular biology and biotechnology research in crop plants. The prescience of the role of biotechnology in agriculture led to a bigger responsibility for this centre and it was elevated as National Research Centre on Plant Biotechnology in the year 1993 (Now NIPB).

    Post : Research Associate

  • 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

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