Role at a glance
- Salary
- Not Disclosed
- Location
- Hyderabad, India
- Work arrangement
- Remote
- Employment
- Full-time
- Experience
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’).
- Education
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
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Role Summary
The Associate Safety Reporting Specialist assists with the receipt, submission, and tracking of expedited and periodic safety reports for the department's projects. The role also supports management in producing project metrics and participates in safety reporting projects and programs.
What You'll Do
- Receive, prepare, and submit safety reports to applicable parties, ensuring compliance with regulatory timelines and country legislation.
- Track all expedited and periodic safety report submissions, retain evidence of submission, and alert the lead or line manager to quality...
- Develop project management skills by supporting an assigned lead, and may lead small projects.
- Liaise with relevant teams around safety reporting tasks and assist the assigned lead as required.
- Run reports and ensure repositories and systems are maintained with up-to-date contact information.
- Ensure regulatory submission files and filing processes are prepared, maintained, and archived per the organization's WPDs or applicable...
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Bachelor's degree or equivalent with roughly 0 to 2 years of comparable experience, plus basic medical terminology and global safety reporting knowledge.
Required
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience comparable to 0 to 2 years
- Basic knowledge of medical terminology
- Good written and verbal communication skills
- Proficiency in Microsoft Office programs
- Basic understanding of safety database functionality
- Basic knowledge of procedural documents
- Working knowledge of global safety reporting requirements (including FDA regulations and guidelines)
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join Us as a Associate Safety Reporting Specialist – Make an Impact at the Forefront of InnovationAt 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 You'll 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 organization's WPDs or applicable client SOPs.
• Assist the manager in the collation of metrics.
Education and Experience Requirements:
• Bachelor's 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.
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.