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    Job · 22455608

    Thermo Fisher Scientific logo

    Safety Reporting Specialist

    Thermo Fisher Scientific · Hyderabad · onsite · Posted 1d ago

    Undisclosed5–10 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Work Schedule

    Standard (Mon-Fri)

    Environmental Conditions

    Office

    Job Description

    Join Us as a Associate Safety Reporting Specialist - Make an Impact at the Forefront of Innovation

    At Thermo Fisher Scientific, you ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

    The Associate Safety Reporting Specialist assists in the receipt, submission, and subsequent tracking of expedited and periodic safety reports pertaining to the department s projects. Supports management in producing project metrics as required. Participates in projects and programs relating to safety reporting.

    We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

    What Youll Do:
    - Receive, prepare, and submit safety reports to applicable parties, ensuring compliance with regulatory timelines and country legislation.
    - Track all expedited/periodic safety report submissions, ensuring retention of evidence of submission. Alert your lead and/or line manager to any quality or timeline issues.
    - Develop project management skills by acting as support to an assigned lead, and may also lead small projects.
    - Liaise with relevant teams around safety reporting tasks and assist the assigned lead as required.
    - Run reports and ensure that repositories/systems are maintained with up-to-date contact information. Provide ad hoc administrative support as and when required.
    - Ensure regulatory submission files and filing processes are prepared, set up, maintained, and archived as per the organizations WPDs or applicable client SOPs.
    - Assist the manager in the collation of metrics.

    Education and Experience Requirements:
    - Bachelors degree or equivalent and relevant formal academic / vocational qualification
    - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years ).

    In some cases an equivalency, consisting of a combination of appropriate education, training
    and/or directly related experience, will be considered sufficient for an individual to meet the
    requirements of the role.

    Knowledge, Skills, Abilities:
    - Basic knowledge of medical terminology
    - Good written and verbal communication skills
    - Proficiency in Microsoft Office programs and a basic understanding of safety database functionality
    - Basic knowledge of procedural documents and working knowledge of global safety reporting requirements (including FDA regulations and guidelines)
    - Good organizational and time management skills
    - Strong attention to detail and accuracy with orientation toward careful and meticulous work
    - Possess the maturity to handle sensitive information and data effectively
    - Ability to interact effectively with all levels of the organization
    - Ability to work effectively within a team

    Working Environment:
    Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

    - Work is performed in an office/ laboratory and/or a clinical environment.
    - Exposure to biological fluids with potential exposure to infectious organisms.
    - Exposure to electrical office equipment.
    - Personal protective equipment required such as protective eyewear, garments and gloves

    Why join us
    When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You ll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.

    Apply today to help us deliver tomorrow s breakthroughs.



    Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Skills

    Administrative SupportMedical Terminologyclinical researchclinical trialstime management skillsmicrosoft officeoffice equipmentProject ManagementResearchCommunication SkillscompliancePharmaceutical

    About Thermo Fisher Scientific

    Thermo Fisher Scientific logo

    Thermo Fisher Scientific

    Biotechnology

    4.8k+

    employees

    1956

    70 years old

    Waltham,Massachusetts

    United States

    About

    Thermo Fisher Scientific enables their customers to make the world healthier, cleaner and safer.

    Industries

    BiotechnologyBiotech & Life sciencesInternetAnalytics & KPOPharma

    Employee ratings

    1,052 reviews

    3.8/ 5

    Culture

    3.7

    Career growth

    3.0

    Work-life

    3.8

    Employees rate it well for

    Work Life Balance177Work Culture134Senior Management98Salary96Career Growth65

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