[Remote] Senior Drug Safety Associate, Pharmcoviligence - US - Remote
Note: The job is a remote job and is open to candidates in USA. Worldwide Clinical Trials is a global, midsize CRO committed to improving lives through innovative approaches. The Senior Drug Safety Associate will be responsible for the collection, processing, evaluation, and reporting of Serious Adverse Event data, serving as a lead on complex studies while mentoring junior staff.
Responsibilities
ā¢ Author Safety Management Plan for assigned studies
ā¢ Review incoming SAE data for completeness and accuracy
ā¢ Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
ā¢ Generate queries for missing or unclear information and follow-up with sites for resolution
ā¢ Perform QC of SAEs processed by other PV Associates
ā¢ Generate regulatory reports and perform safety submissions as needed
Skills
ā¢ Excellent understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
ā¢ Excellent understanding of computer technology, and management of relational database systems, including extraction of data
ā¢ Positive attitude and ability to interact diplomatically and professionally with internal and external customers in a global environment
ā¢ Excellent organizational skills and ability to handle multiple competing priorities within tight timelines
ā¢ Bachelor's degree in a science-related field, or nursing, or equivalent
ā¢ Minimum of 5 years of pharmacovigilance experience (pre-approval clinical trials)
ā¢ Equivalent combination of relevant education and experience
ā¢ Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
ā¢ Excellent written and verbal communication skills
ā¢ Excellent organizational skills and attention to detail
ā¢ Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines
ā¢ Ability to work independently, prioritize work effectively and work successfully in matrix team environment
ā¢ Ability and willingness for potential limited travel (domestic and international) as needed (attend Investigator Meeting, project kick-off meeting and/or bid defense meeting)
ā¢ Fluent in written and verbal English
Company Overview
ā¢ Worldwide Clinical Trials is a global CRO that provides preclinical and Phase I-IV clinical development services to pharmaceutical industry. It was founded in 1986, and is headquartered in Morrisville, North Carolina, USA, with a workforce of 1001-5000 employees. Its website is https://www.worldwide.com.
Company H1B Sponsorship
ā¢ Worldwide Clinical Trials has a track record of offering H1B sponsorships, with 1 in 2024, 5 in 2023, 3 in 2022, 2 in 2021, 2 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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Responsibilities
ā¢ Author Safety Management Plan for assigned studies
ā¢ Review incoming SAE data for completeness and accuracy
ā¢ Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
ā¢ Generate queries for missing or unclear information and follow-up with sites for resolution
ā¢ Perform QC of SAEs processed by other PV Associates
ā¢ Generate regulatory reports and perform safety submissions as needed
Skills
ā¢ Excellent understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
ā¢ Excellent understanding of computer technology, and management of relational database systems, including extraction of data
ā¢ Positive attitude and ability to interact diplomatically and professionally with internal and external customers in a global environment
ā¢ Excellent organizational skills and ability to handle multiple competing priorities within tight timelines
ā¢ Bachelor's degree in a science-related field, or nursing, or equivalent
ā¢ Minimum of 5 years of pharmacovigilance experience (pre-approval clinical trials)
ā¢ Equivalent combination of relevant education and experience
ā¢ Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
ā¢ Excellent written and verbal communication skills
ā¢ Excellent organizational skills and attention to detail
ā¢ Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines
ā¢ Ability to work independently, prioritize work effectively and work successfully in matrix team environment
ā¢ Ability and willingness for potential limited travel (domestic and international) as needed (attend Investigator Meeting, project kick-off meeting and/or bid defense meeting)
ā¢ Fluent in written and verbal English
Company Overview
ā¢ Worldwide Clinical Trials is a global CRO that provides preclinical and Phase I-IV clinical development services to pharmaceutical industry. It was founded in 1986, and is headquartered in Morrisville, North Carolina, USA, with a workforce of 1001-5000 employees. Its website is https://www.worldwide.com.
Company H1B Sponsorship
ā¢ Worldwide Clinical Trials has a track record of offering H1B sponsorships, with 1 in 2024, 5 in 2023, 3 in 2022, 2 in 2021, 2 in 2020. Please note that this does not guarantee sponsorship for this specific role.
Apply tot his job
Apply To this Job