ThermoFisher is Hiring for Safety Specialist:Hello friends if you are Life science graduate fresher or experience of then this is the best job opportunity for youThermofisher is Hiring for Safety Specialist.Here you will get industries best salary upto 5Lakh per year.And best part its a Work From Home job.If you are intrusted in this job then read the details below and apply ASAP.

About Company

ThermoFisher Scientific Inc., specializes in life sciences and clinical research. It provides worldwide services in biotechnology, pharmaceuticals, diagnostics, laboratories,analytical instruments,and clinical development solutions. The is located in Headquartered in America.ThermoFisher gives equal opportunity to all candidates and employers. If you are qualified for the job application then you will get a equal opportunity without the discrimination of sex, race , gender.

ThermoFisher Freshers Hiring 2024

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• Job Overview

1. Manages daily Pharmacovigilance (PV) tasks in a highly regulated setting with strict deadlines.
2. Collaborates with project teams, clients, investigators, and vendors. Assists in developing procedures, prepares for audits, and participates in meetings.
3. Responsibilities include collecting, monitoring, assessing, and researching safety data.
4. Coordinates PV activities like data entry, coding adverse events, case reviews, and regulatory reporting.

• Education Qualification and Experience that Required for the Job Role

1. A Bachelor’s degree or similar academic or qualification is required, along with relevant previous experience that equips the individual with the necessary knowledge, skills, and abilities (equivalent to 2+ years).
2. In certain instances, a combination of suitable education, training, and directly related experience may also meet the qualifications needed for the position.
3. Bachelor’s degree or equivalent academic/vocational qualification is necessary.
4. Previous experience of at least 2+ years that provides the required skills and knowledge is required.
5. Alternative combinations of education, training, and relevant experience may be considered in some cases to meet the role’s requirements.

• Job Description

1. Responsibilities encompass collecting, monitoring, assessing, evaluating,researching, and tracking safety data.
2. Assists in developing departmental and project-specific procedures and processes.
3. Prepares for and participates in audits, kick-off meetings, and investigator meetings as required.
4. Coordinates PV activities including data entry, coding adverse events, conducting case reviews, follow-up procedures, report tracking, and regulatory reporting.
5. Engages in daily Pharmacovigilance (PV) tasks in a highly regulated environment with strict deadlines.
6. Collaborates effectively with project team members, client contacts, investigators,adverse evenreporters, and third-party vendors.
7. Responsible for gathering, monitoring, evaluating, researching, and keeping track of safety information.
8. Assists in creating specific procedures and processes for both departmental and project-related needs.
9. Prepares for and actively participates in audits, as well as kick-off and investigator meetings as necessary.
10. Manages Pharmacovigilance activities such as entering data, coding adverse events, conducting case reviews, following up on cases, tracking reports, and handling regulatory reporting.
11. Performs daily Pharmacovigilance tasks within a tightly regulated environment,adhering to strict deadlines.
12. Works closely and effectively with project team members, client contacts,investigators, individuals reporting adverse events, 5678iand external vendors.

• Job role and Responsibilities

1. Engages in daily Pharmacovigilance (PV) activities, including participating in on-call duties for specific projects to ensure round-the-clock case intake from investigative sites.
2. Maintains a thorough medical understanding of relevant therapeutic areas and disease conditions.
3. Conducts thorough reviews of entered cases to ensure quality, consistency, and accuracy, including peer report evaluations.
4. Regularly reviews regulatory and pharmacovigilance publications and information sources to stay current with evolving regulations, practices, procedures, and proposals.
5. Provides mentoring and guidance to less experienced staff members.
6. Prepares and updates regulatory safety reports as required.
7. Assists in the routine implementation and coordination of projects such as Clinical
   Trials and Endpoint Assessment Committee/Data Safety Monitoring Committeeactivities.
8. This includes presenting at client and investigator meetings, and reviewing metrics and budget considerations.

• Skills and Knowledge Required for the job

1. Has in-depth knowledge of specific therapeutic areas relevant to processing Adverse Events (AEs).
2. Possesses a general understanding of pathophysiology and how diseases develop.
3. Maintains a positive and professional attitude even in challenging situations.
4. Demonstrates strong critical thinking and problem-solving abilities.
5. Proficient in using computers and navigating multiple databases.
6. Has previous experience with Microsoft Office tools such as Outlook, Word, and Excel.
7. Commands a proficient level of English and can translate information into local languages when necessary.
8. Capable of managing and prioritizing various tasks while meeting tight deadlines with minimal supervision.
9. Exhibits good oral and written communication skills, including the ability to Rephrase information effectively.
10. Understands the importance of adhering to procedural documents and regulatory requirements.
11. Pays strong attention to detail in all tasks undertaken.
12. Works effectively within a team to achieve common objectives.

How to apply
Intrested candidate should read the overview of job and apply accordingly with updated resume .

Upload the updated resume on the given link below.

Apply Link : Click Here

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