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Complaints Intake Analyst German/Dutch Speaking
MAIDENHEAD, BERKSHIRE
...Regulatory Affairs and PharmacovigilanceSupports more complex complaints that are escalatedServe as a Subject Matter Expert for a designated product(s) within the team when requiredWhere applicable, decide whether a replacement, credit, or warranty claim is warranted, and notify the...
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Senior Manager, Global Patient Safety
54767
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...process and global pharmacovigilance regulations, systems, and processes. Extensive knowledge of the adverse event lifecycle. Does this sound like you? Apply now to take your first step towards living the Regeneron Way We have an inclusive and diverse culture that provides comprehensive...
Mechanical and Electrical Building Technician
HERTFORDSHIRE, EAST ANGLIA, UNITED KINGDOM
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their...
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SOUTH EAST
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Senior Manager, Global Patient Safety Scientist
53398
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments You demonstrated the ability to contribute positively to a healthy, diverse and inclusive team environment. Excellent organizational and relationship leadership skills Strong technical and...
Associate Director, Global Patient Safety Scientist - Immunology & Inflammation
64085
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments. Ability to work with a safety system database. Ability to prioritize and multitask to meet deliverables. Ability to effectively communicate (verbal and written) safety findings. To be...
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Senior Manager, Global Patient Safety Scientist - Oncology
56604
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments Ability to work with a safety system database for purposes of medical case review and simple queries Able to be proactive and self-disciplined, you can meet deliverables, and effectively...
Director, Global Patient Safety Sciences - Solid Oncology
52696
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required. Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest. A proven...
Associate Director, Global Patient Safety
63214
UXBRIDGE, LONDON , UXBRIDGE, LONDON
Regeneron is seeking an Associate Director in Global Patient Safety, this position is a pivotal role within Regeneron's Global Patient Safety organization, specifically in the Case Evaluation & Reporting area. We need someone who will coordinate pharmacovigilance operations, ensuring efficient...
Business Development Manager UK&I
43382
LONDON , LONDON , LONDON , LONDON
...regulatory, and pharmacovigilance solutions. Strong results-driven attitude. Ability to work in a dynamic, global environment. Skilled in finding and closing new business deals. Responsible and diplomatic. Excellent English communication and presentation skills. Willingness to travel...
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CRA II - 5 Month FTC
36566
; HOMEWORKING, , UK; HOMEWORKING,
...violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): o Assesses site processes o Conducts Source Document Review of appropriate site source documents and medical records o Verifies required clinical data entered in the case report form...
Freelance SrCRA role, 1 FTE for 5 month period. UK & Ireland sites
44619
; HOMEWORKING, , UK; HOMEWORKING,
...violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): o Assesses site processes o Conducts Source Document Review of appropriate site source documents and medical records o Verifies required clinical data entered in the case report form...
Senior CRA / CRA II - Sponsor Dedicated - Cardiovascular - Scotland / North East (United Kingdom)
45434
; HOMEWORKING, , UK; HOMEWORKING,
...violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes Conducts Source Document Review of appropriate site source documents and medical records Verifies required clinical data entered in the case report form (CRF) is...
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