For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Medical writing, Regulatory affairs, Clinical research, Project management, ICH E3
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Principal Pharmacovigilance Specialist, Case Processing
Raleigh, North Carolina, United States · Hybrid
Mid level$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Makati City, National Capital District, Philippines · Hybrid
Mid level$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Medical terminology, Pharmacology, Pathophysiology, Regulatory compliance, Pharmacovigilance
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Remote opportunity- Swedish speaking Medical Information Specialist - 12 month contract
North Yorkshire, England, United Kingdom · Hybrid
Entry level$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Medical information, Pharmacovigilance, Swedish, English, Regulatory compliance
CEE, Regulatory Affairs Specialist and Pharmacovigilance Officer
Podgorica, Montenegro · Hybrid
Mid level$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Senior Pharmacovigilance Specialist, case processing
Makati City, National Capital District, Philippines · Hybrid
Mid level$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Senior Pharmacovigilance Coordinator, Case Processing
Makati City, National Capital District, Philippines · Hybrid
Entry level$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Pharmacovigilance, Case processing, Data entry, Regulatory authority database searches, Inbox triage
Graduate opportunity- German speaking Medical Information Specialist
City of Zagreb, Zagreb, Croatia · Hybrid
Entry level$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Medical information, Pharmacovigilance, Regulatory affairs, Drug safety, Clinical research
Raleigh, North Carolina, United States · Remote OK
Senior$9M raised
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Pharmacovigilance, Medical writing, Aggregate reporting, Signal management, Risk management plans
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Corporate Tax, Accounting Principles, Microsoft Excel, U.S. GAAP, Tax Compliance
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Business Development, Sales Strategy, Contract Negotiation, Proposal Writing, CRM
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
Skills: Clinical Monitoring, Site Management, GCP, ICH Guidelines, EDC
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance …
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Full-time
bachelor degree, postgraduate degree
Posted 5d ago
~40 hrs/week
Responsibilities
The Pharmacovigilance Specialist manages individual case safety reports, performs initial assessments of seriousness and expectedness, and composes accurate medical narratives. They ensure all expedited regulatory reporting criteria are met and maintain compliance with internal SOPs and global safety regulations.
Requirements
Candidates must hold a Bachelor's degree in life sciences and possess at least two years of related work experience. Strong communication skills, attention to detail, and a basic knowledge of pharmacovigilance are essential for this role.
Full job description
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
The Pharmacovigilance (PV) Specialist, Case Processing manages individual case safety reports, performs initial case-level assessment of expectedness, confirms seriousness, composes accurate and thorough medical narratives, and generates queries for missing or unclear information. The PV Specialist ensures all cases meeting expedited regulatory reporting criteria are submitted to regulatory authorities in accordance with internal guidelines, Working Practices, SOPs, and applicable safety regulations. The PV Specialist maintains distinctive quality and commitment as the operating philosophy in carrying out all processes, and continually seeks out ways to enhance customer service experience both internally and externally.
Essential Functions:
Responsible for daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level.
Perform case follow up activities such as identification of information to be collected during follow-up.
Creating and reviewing case narratives.
Providing client notifications as required for case management.
Supporting and contributing to the development of training materials and training delivery.
Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs.
Acquire and maintain an up-to-date knowledge of global safety regulations for medicines.
Peer reviews of cases for quality, consistency, and accuracy as needed.
Other duties as assigned
Necessary Skills and Abilities:
Strong verbal, written and interpersonal communication skills.
High level of accuracy and attention to detail.
Ability to identify and resolve problems in a timely manner.
Able to work independently and collaboratively in a multi-disciplinary team.
Excellent organization and prioritization skills; able to multitask.
Basic knowledge of Pharmacovigilance.
Educational Requirements:
Required: a Bachelor's degree in life sciences.
Preferred: advanced degree, RN, RPh, PharmD or equivalent.
Experience Requirements:
Two years of related work experience.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.
End-to-end bespoke solutions that de-risk & accelerate our partners' and sponsors' drug and device development programs
Industry
Business Consulting and Services
Company size
1,001-5,000 employees
Founded
2001
Headquarters
Raleigh, North Carolina
LinkedIn followers
200,357
Total funding
$9M
At ProPharma, we help pharmaceutical, biotechnology, and medical device companies bring life-changing therapies to market. From early development through clinical, regulatory approval, and commercialization, we provide expert guidance to navigate complex challenges and accelerate success.
Our mission is simple: improving patient health and safety by delivering the highest-quality regulatory, compliance, clinical research, pharmacovigilance, and medical information services throughout the entire product lifecycle.
With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risks and accelerates high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!
Offices: 107 W Hargett St, Raleigh, North Carolina 27601, US · Olliver, Richmond, North Yorkshire DL10 5HX, GB · Schipholweg 59, P.O. Box 255, Leiden, AG 2316 ZL, NL · Siemensdamm 62, Berlin, Germany 13627, DE · Solnavägen 3H, 113 63 Stockholm, Sweden, Stockholm, Stockholm County SE -112, SE
End-to-end bespoke solutions that de-risk & accelerate our partners' and sponsors' drug and device development programs
Industry
Business Consulting and Services
Company size
1,001-5,000 employees
Founded
2001
Headquarters
Raleigh, North Carolina
LinkedIn followers
200,357
Total funding
$9M
At ProPharma, we help pharmaceutical, biotechnology, and medical device companies bring life-changing therapies to market. From early development through clinical, regulatory approval, and commercialization, we provide expert guidance to navigate complex challenges and accelerate success.
Our mission is simple: improving patient health and safety by delivering the highest-quality regulatory, compliance, clinical research, pharmacovigilance, and medical information services throughout the entire product lifecycle.
With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risks and accelerates high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!
Offices: 107 W Hargett St, Raleigh, North Carolina 27601, US · Olliver, Richmond, North Yorkshire DL10 5HX, GB · Schipholweg 59, P.O. Box 255, Leiden, AG 2316 ZL, NL · Siemensdamm 62, Berlin, Germany 13627, DE · Solnavägen 3H, 113 63 Stockholm, Sweden, Stockholm, Stockholm County SE -112, SE