Drug Safety Associate II Pharmacovigilance - US - Remote
Drug Safety Associate II Pharmacovigilance - US - Remote
Posted on :
20-01-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
Job Title: Drug Safety Associate II Pharmacovigilance US Remote
Job Location: England UK
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level: Entry level
Who We Are
We’re a global midsize CRO that pushes boundaries innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials and we are a global team of over 3500 experts bright thinkers dreamers and doers and together we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our handson accessible leaders to our cohesive and supportive teams we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
To view our other roles check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide visit or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and to that end we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included they can be more creative innovative and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race color ethnicity ancestry religion national origin gender sex gender identity or expression sexual orientation age citizenship marital or parental status disability military status or other class protected by applicable law.
We’re a global midsize CRO that pushes boundaries innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials and we are a global team of over 3500 experts bright thinkers dreamers and doers and together we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our handson accessible leaders to our cohesive and supportive teams we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
- SUMMARY: Collection processing and evaluation of the information on Serious Adverse Events (SAEs) that are reported to the Company including preparation of summary narratives of the information contained in the case assigning the proper regulatory reporting status and accurately entering the data into Drug Safety Database.* *Assist the Drug Safety Manager/Officer in the preparation of periodic safety reports to be submitted to regulatory authorities worldwide and provide routine database searching extraction and reporting services to the department.* *RESPONSIBILITIES:* Tasks may include but are not limited to: Evaluation of case information determination of the regulatory reporting status of each case and accurate entry of case information into the safety database. Provide retrieval and reporting of data from the WCT’s global safety database. Ad hoc data extraction and reporting as requested by internal and external customers. Support to the Safety Officer in the generation of Safety Update Reports (ASR Periodic Line listings) and other regulatory reports. Interaction with other functions (ClinOps Data Mangement) including database reconciliation. Assures that all safety data originated in projects assigned are handled in accordance with WCT global standard operative procedures and local working practices. Act as a support person in the preparation of studyspecific Safety Monitoring Plans in order to gain a deep knowledge of how to handle the SAE cases in the specific study. Contribute in the safety signal generation and evaluation process through safety database searching and extracting. Be always updated on the laws/guidelines/regulations of drug safety in the region. Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily allinclusive. *OTHER SKILLS AND ABILITIES: * Good understanding of medical and scientific terminology of the principles of clinical assessment of adverse drug events of international regulations and of reporting requirements. Good understanding of computer technology and management of relational database systems including extraction of data. Good oral and written communication skills. High skills in time management and organization. Fluency in written and verbal English *REQUIREMENTS:* Bachelor degree in a sciencerelated field or nursing or equivalent. Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency level of responsibility and ability to work independently.
To view our other roles check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide visit or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and to that end we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included they can be more creative innovative and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race color ethnicity ancestry religion national origin gender sex gender identity or expression sexual orientation age citizenship marital or parental status disability military status or other class protected by applicable law.
/jobs/view/153b1724c492bbb63dffcbaff0d1f89e
Employment Type
Full Time
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
