Job details
Job type full-time
Full job description
Sr safety & pv specialist - (21011332) description
Senior safety & pharmacovigilance specialist
Come discover what our 25,000+ employees already know: work here matters everywhereWe’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.
As a part of the syneos health team, you’ll help us deliver results for a rewarding reason – we improve patients’ lives around the worldBecause to us, a patient isn’t just a number, they’re our family, friends, and neighbors.
Why syneos health
#syneoshealthlife means we’re committed to our total self culture – where everyone can authentically be themselvesOur total self culture is what unites us globally, and we know every person’s unique contributions make a difference.
We believe our success is a direct result of the people who are driving it – you! we value your dedication to care for our customers and patients, so we want to focus on taking care of youThat’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
We are continuously building the company we all want to work for and our customers want to work withWhy? because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job responsibilities
Coordinating workflow to ensure delivery of project.
Escalates issues with project deliverables, finance and quality to safety program delivery lead/manager or line manager as appropriate in a timely manner
Has an understanding of financial measures, work orders, performance metrics (including quality parameters, monthly budget reports, and changes in scope) and project budgets.
Prepares safety management plan.
Assists in the preparation and participates in internal project review meetings as required.
May enter information into pvg quality and tracking systems for receipt and tracking icsr.
May process icsrs according to standard operating procedures (sops) and project/program- specific safety plans.
O triages icsrs, evaluates icsr data for completeness, accuracy, and regulatory report ability.
O enters data into safety database.
O codes events, medical history, concomitant medications and tests.
O compiles complete narrative summaries.
O assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved.
O participates in the generation of timely, consistent and accurate reporting of expedited reports in accordance with applicable regulatory requirements.
O coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases
Ensures distribution of all required individual expedited and periodic reports for both clinical and post-marketing projects to the safety submissions team if contracted to submit the reports.
Provides training of investigators on icsr reporting
Participate in audits/inspections as required
Ensures all relevant documents are submitted to the trial master file (tmf) as per company sop/sponsor requirements for clinical trials and the pharmacovigilance system master file for post-marketing programs as appropriate.
Maintains understanding and compliance with sops, work instructions (wis), global drug/biologic/device regulations, gcps, ich guidelines, gvp, project/program plans and the drug development process.
Qualifications
What we’re looking for
Bachelor’s degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.
Safety database systems and knowledge of medical terminology required
In depth understanding of clinical trial process across phases ii-iv and/or post-marketing safety requirements, ich gcp, gvp and regulations related to safety and pharmacovigilance
Proficiency in microsoft office suite (word, excel and powerpoint), visio, email (outlook), teamshare (or other management/shared content/workspace) and internet.
Ability to work independently and in a team environment
Strong communication, presentation, interpersonal skills, both written and spoken
Strong organizational skills with proven ability to prioritize and work on multiple tasks and projects
Detail oriented with a high degree of accuracy and ability to meet deadlines
Able to make effective decisions
Minimal travel may be required (up to 10%)
Get to know syneos health
We are the only full-service biopharmaceutical solutions company in the worldThat means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it mostLearn more about syneos health.
Additional information:
Tasks, duties, and responsibilities as listed in this job description are not exhaustiveThe company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilitiesEquivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the job descriptionThe company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described aboveFurther, nothing contained herein should be construed to create an employment contractOccasionally, required skills/experiences for jobs are expressed in brief termsAny language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the eu equality directive, in relation to the recruitment and employment of its employeesThe company is committed to compliance with the americans with disabilities act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
As a healthcare company we have an important responsibility to protect individual and public healthThis position will require individuals to be fully vaccinated against covid-19 as part of their job responsibilities, unless an exemption can be confirmed based on a medical condition or sincerely held religious beliefSubmission & approval of an exemption does not guarantee that an exemption can be accommodated.
This job excludes co applicants.
Primary location: north america - us home-based
Job: safety & pharmaco
Schedule: full-time
Travel: no
Employee status: regular
