Associate Ii, Pharmacovigilance - United Kingdom - Worldwide Clinical Trials

Worldwide Clinical Trials

Verified Company

United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Requisition Number7925**
Employment Type:Regular**
Who we are

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality.

Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers.

From our hands-on, 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

What you will do

Author Safety Management Plan for assigned studies. Attend internal and client meetings as appropriate and present at Investigator Meetings
Review incoming SAE data for completeness and accuracy. Perform QC of SAEs processed by other PV Associates
Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
Generate queries for missing or unclear information and followup with sites for resolution. Generate regulatory reports and perform safety submissions as needed. Prepare and submit periodic safety reports as needed

What you will bring to the role

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
Positive attitude and ability to interact diplomatically and professionally with internal and external customers in a global environment
Excellent organization skills and ability to handle multiple competing priorities within tight timelines

Your background

Bachelor's degree in a sciencerelated field, nursing, or equivalent
Minimum of 3 years of pharmacovigilance experience (preapproval clinical trials)
Excellent written and verbal communication skills

We love knowing that someone is going to have a better life because of the work we do.

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