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COMPANY

ProPharma Group

HQ: Raleigh, NC source · propharmagroup.com ↗

Status: Acquired, now part of Odyssey Investment Partners · How status works

63 open jobs · last seen Oct 23, 2026 · 1 source

Keywords: medical device

Location: Raleigh, NC · source · Oct 15, 2026

Profile checked Oct 10, 2026

63+4 patient-care hiddenOpen jobs

Hiring

TitleLocation (from posting)Employer postedFirst seen
German Speaking Medical Information Specialist - Graduate Opportunity3 locations (listed on the posting)Oct 23, 2026Oct 23, 2026
Freelance SCRA - IRE - 0.8FTEDublinOct 22, 2026Oct 22, 2026
Registered Nurse-Clinical Trial-New Glasgow, Nova Scotia CANCanadaOct 22, 2026Oct 23, 2026
Compliance and Quality Assurance Consultant - Product Quality Complaints - Permanent role4 locations (listed on the posting)Oct 21, 2026Oct 15, 2026
GMP Compliance and Quality Assurance Auditor and SOP Technical Writer.United StatesOct 21, 2026Oct 22, 2026

See all 63 jobs

Timeline

  1. Board tracked Radar started tracking this company’s job board (67 open jobs at last check). source ↗

Open jobs 63

4 patient-care jobs hidden (phlebotomy, plasma-center, nursing and similar care roles; 67 open jobs in total).

TitleLocation (from posting, not HQ)Employer postedFirst seenLevel
German Speaking Medical Information Specialist - Graduate Opportunity3 locations (listed on the posting)Oct 23, 2026Oct 23, 2026Not stated
Freelance SCRA - IRE - 0.8FTEDublinOct 22, 2026Oct 22, 2026Not stated
Registered Nurse-Clinical Trial-New Glasgow, Nova Scotia CANCanadaOct 22, 2026Oct 23, 2026Not stated
Compliance and Quality Assurance Consultant - Product Quality Complaints - Permanent role4 locations (listed on the posting)Oct 21, 2026Oct 15, 2026Mid
GMP Compliance and Quality Assurance Auditor and SOP Technical Writer.United StatesOct 21, 2026Oct 22, 2026Not stated
Principal Pharmacovigilance SpecialistUnited StatesOct 21, 2026Oct 22, 2026Not stated
Pharmcovigilance Case processing & Quality Product Complaint SpecialistStockholmOct 21, 2026Oct 22, 2026Not stated
Principal Consultant - Product Lifecycle Management - Permanent position6 locations (listed on the posting)Oct 19, 2026Oct 17, 2026Not stated
Quality SpecialistIndiaOct 16, 2026Oct 16, 2026Not stated
Interim VP, Regulatory AffairsUnited StatesOct 12, 2026Oct 12, 2026Executive
Principal Medical Writer (Device)United StatesOct 12, 2026Oct 12, 2026Senior
Quality Record Investigation ConsultantUnited StatesOct 12, 2026Oct 13, 2026Mid
Quality Record Investigation Lead ConsultantUnited StatesOct 12, 2026Oct 13, 2026Senior
PV Specialist, Case ProcessingMakati CityOct 9, 2026Oct 9, 2026Mid
Director, Business Development- Quality and Compliance10 locations (listed on the posting)Oct 8, 2026Oct 8, 2026Senior
Director, Promotional Review & Labeling ServicesUnited StatesOct 7, 2026Oct 8, 2026Senior
Registered Nurse-Clinical Trial-Chandler, ArizonaUnited StatesOct 6, 2026Oct 6, 2026Entry
Environmental Monitoring Program Lead ConsultantUnited StatesOct 5, 2026Oct 6, 2026Senior
Program Lead/Sterility Assurance Review Senior ConsultantUnited StatesOct 5, 2026Oct 6, 2026Senior
Sterility Assurance Senior ConsultantUnited StatesOct 5, 2026Oct 6, 2026Senior
Senior Clinical Research Associate - Alzheimer's DiseaseUnited StatesOct 1, 2026Oct 5, 2026Senior
Senior Project Manager - Rare DiseaseUnited StatesSep 30, 2026Oct 5, 2026Senior
Image Service Product Owner (Consultant)United StatesSep 30, 2026Oct 5, 2026Mid
Compliance and Quality Assurance Consultant - Permanent position2 locations (listed on the posting)Sep 28, 2026Oct 5, 2026Senior
Safety Specialist, Pharmacovigilance Case ProcessingSwedenSep 28, 2026Oct 5, 2026Mid
Principal Medical WriterUnited StatesSep 25, 2026Oct 5, 2026Senior
Director, Medical WritingUnited StatesSep 24, 2026Oct 5, 2026Senior
Pharmacovigilance Client Account Manager, Client ServicesUnited StatesSep 24, 2026Oct 5, 2026Mid
Senior Pharmacovigilance Client Account Manager, Client ServicesUnited StatesSep 24, 2026Oct 5, 2026Senior
Pharmacovigilance Safety Surveillance SpecialistMakati CitySep 23, 2026Oct 5, 2026Entry
Senior Pharmacovigilance Specialist, Regulatory Intelligence and Submissions3 locations (listed on the posting)Sep 23, 2026Oct 5, 2026Senior
Medical Information AssistantBelgradeSep 23, 2026Oct 5, 2026Entry
Senior Clinical LeadRaleighSep 23, 2026Oct 5, 2026Senior
Quality Documentation SpecialistIndiaSep 23, 2026Oct 5, 2026Mid
Director, Business Development (Regulatory Sciences)United StatesSep 23, 2026Oct 5, 2026Senior
Computer System Validation EngineerBelgradeSep 23, 2026Oct 5, 2026Entry
Regulatory Promotional Review ConsultantUnited StatesSep 23, 2026Oct 5, 2026Mid
Cell & Gene Therapy SME - USUnited StatesSep 23, 2026Oct 5, 2026Senior
Principal Medical Writer (Consultant)United StatesSep 23, 2026Oct 5, 2026Senior
Director, Business Development (Medical Information Services)United StatesSep 23, 2026Oct 5, 2026Senior
Multilingual Medical Information Specialist, JapanTokyoSep 23, 2026Oct 5, 2026Mid
Multilingual Medical Information Specialist - Korean/EnglishMelbourneSep 23, 2026Oct 5, 2026Mid
Senior Pharmacovigilance Consultant, Alliance Management10 locations (listed on the posting)Sep 23, 2026Oct 5, 2026Senior
Freelance/Contract - GMP Facility management ConsultantSwedenSep 23, 2026Oct 5, 2026Mid
Freelance/Contract Principal Quality Assurance ConsultantSwedenSep 23, 2026Oct 5, 2026Senior
Registered Nurse-Clinical Trial-Alexandria, VAUnited StatesSep 23, 2026Oct 5, 2026Entry
Executive Assistant & Medical Affairs Project Coordinator (Onsite, Wilmington, DE)United StatesSep 23, 2026Oct 5, 2026Mid

Level (Entry/Mid/Senior/Executive) is estimated from the job title and required years of experience. Descriptions are short excerpts (about the first 60 words) of the posting plus skills picked out of it; use Read full posting for the complete text.

All 63 jobs →

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LinkedIn page linked from the company's own site: source · seen 2026-10-18

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