Drug Safety
Integrated Resources Inc
Drug Safety A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Case Processing: 75% of time Definition: The completion of full case information on the database, culminating in Quality Review to ensure accuracy and completeness. Activities Include: Triage of incoming cases to determine seriousness for prioritization of daily workflow (to be discussed re triage specialist) Confirmation of Safety Coordinator case registry data Database searches as necessary Completion of literature searches as necessary Completion of remaining case data entry, including narrative or auto-narrative Completion of risk and quality (label, approval, manual coding & quality review steps) Clarification of unclear or illegible information from the LSO or Call Centre Discuss source documents, coding conventions and ad-hoc queries with Medical Assessment Physician Completion of protocol request forms as necessary Preparation of deviation memo as necessary Request deletions as necessary Single case unblinding Processes and Procedures: 5% of time Definition: Continuing awareness of company procedures and guidelines to maintain regulatory compliance. Activities Include: Standard Operating Procedures and Working Practices Department guidance documents MedDRA coding dictionary and MedDRA points to consider Understand relevant safety implications regarding contracts with operating companies and/or marketing partners Review and make suggestions for system and procedure enhancements 5% of time = Project Work, Audits, Inspections and other Ad-hoc Integrated Resources
$21.7 per hour
...industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving... ...with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards...SuggestedContract workLocal areaWorldwideFlexible hours$18 per hour
...industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving... ..., and location. Education No degree required About Safety Assessment Charles River is committed to helping our partners...SuggestedContract workWork at officeLocal areaWorldwideFlexible hours$5,000 per month
...Pharmacist you will: Evaluate physician medication orders for drug appropriateness, correct dosage, potential drug interactions,... ...of practice Knowledge of drug therapy guidelines, medication safety practices, and regulatory standards (CMS, DEA, FDA)....SuggestedFull timeMonday to FridayFlexible hoursShift workWeekend work- ...both expedited and periodic reports. Provides integrated strategic safety expertise to clinical development programs. Performs active... ...identification and analysis of safety signals, to define emerging drug safety profiles of all products and drive patient risk management...Suggested
- ...regulatory guidance documents, to ensure compliance with worldwide safety regulations and corporate policies. PRINCIPAL RESPONSIBILITIES:... ...Practical Nurse without Bachelors degree but with knowledge of Drug Safety usually exhibited by minimum 5 years experience in...SuggestedContract workLocal areaWorldwide
$22 per hour
...industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving... ...is preferred. Education No degree required About Safety Assessment Charles River is committed to helping our partners...Contract workLocal areaWorldwideFlexible hours$5,000 per month
...Pharmacist you will: Evaluate physician medication orders for drug appropriateness, correct dosage, potential drug interactions,... ...of practice Knowledge of drug therapy guidelines, medication safety practices, and regulatory standards (CMS, DEA, FDA). Proficiency...Full timeLocal areaMonday to FridayFlexible hoursShift workWeekend work- A leading compliance and pharmacovigilance firm is seeking a Compliance Analyst / Drug Safety Case Processing in Horsham, PA. The successful candidate will be responsible for developing compliance metrics, ensuring quality control, conducting User Acceptance Testing, and...
- ...committed minds to help meet your business objectives, irrespective of the stage your business is in. Job Description Job Title: Drug Safety Coordinator I Duration: 6 Months+ Location : Horsham, PA Summary: Responsible for the receipt and data entry of adverse event reports...Work at officeWorldwide
$180k - $200k
...industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving... ..., skills, education, certifications, and location. About Safety Assessment Charles River is committed to helping our partners expedite...Contract workLocal areaRemote workWorldwideFlexible hours- Une entreprise leader dans le domaine de la sécurité médicale recherche un Spécialiste en Saisie de Données pour gérer les rapports d'événements indésirables. Le candidat doit posséder une formation en soins infirmiers ou un diplôme en sciences de la santé, avec une exp...
- Une entreprise de recrutement reconnue dans le secteur de la santé recherche un responsable qualité et conformité en pharmacovigilance. Le candidat idéal aura un diplôme pertinent et plusieurs années d'expérience dans l'industrie, ainsi qu'une expertise en développement...
- Summary: The Scientist role is primarily responsible for aggregate safety analyses and aggregate report writing. He/she will contribute or will be responsible for report writing and/or report ownership related to core safety deliverables including scheduled and ad‑marketing...
- A leading data analysis firm in Horsham, Pennsylvania, is seeking a Scientist to be responsible for aggregate safety analyses and report ownership related to core safety deliverables. The role involves preparing scheduled and ad-hoc safety reports, conducting safety analysis...
$39.11k - $111.11k
...paid internship. If you thrive in a dynamic environment, love problem-solving, and are eager to learn about the intersection of drug safety, global regulations and technology, we want to hear from you! About The Role As a Pharmacovigilance - Operations & Global Process...Fixed term contractInternshipWorldwideRelocationVisa sponsorshipFlexible hoursShift work- Role: Pharmacovigilance QA Auditor Specialist responsible for leading PV internal and external audits, supporting regulatory inspections, and ensuring compliance across GxP and non-regulated areas within Johnson & Johnson's Innovative Medicine division. Responsibilities...Work at office
$5,000 per month
...Pharmacist you will: Evaluate physician medication orders for drug appropriateness, correct dosage, potential drug interactions,... ...of practice Knowledge of drug therapy guidelines, medication safety practices, and regulatory standards (CMS, DEA, FDA). Proficiency...Full timeMonday to FridayFlexible hoursShift workWeekend work$5,000 per month
...Pharmacist you will: Evaluate physician medication orders for drug appropriateness, correct dosage, potential drug interactions,... ...of practice ~ Knowledge of drug therapy guidelines, medication safety practices, and regulatory standards (CMS, DEA, FDA). ~ Proficiency...Full timeFlexible hoursShift workNight shift$109k - $174.8k
Senior Scientist - Data (AI) Scientist, Translational Safety Our expertise in Innovative Medicine is informed and inspired by patients,... ...Office of Chief Medical Officer) organization helping accelerate drug safety prediction across all stages of drug discovery and...Work at officeLocal areaImmediate start- MSD seeks an experienced anatomic pathologist to join our West Point, PA nonclinical drug safety team. You will lead histopathology and postmortem evaluations within a GLP environment and collaborate with toxicology, immunology, and biologics groups to advance safety assessments...
- ...appropriate) with coaching and clear expectations. Collaborate cross-functionally (Clinical Ops, Regulatory, Biostatistics/Data Mgmt, Drug Safety, Translational Medicine, Medical Affairs, etc.) to align and communicate scientific issues. Ensure compliance with regulatory...
- Johnson & Johnson Innovative Medicine is seeking a Pharmacovigilance QA Auditor Specialist to lead PV internal and external audits, support regulatory inspections, and ensure GxP compliance across diverse areas. The role involves collaboration with business partners and...
- ...Description The Animal Technician II, under the guidance of a Vivarium manager, works to support innovative translational models to impact drug safety assessment, development and discovery and improve human health. Under the direction of a manager or assigned technical staff...For contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work
$117k - $201.25k
...scientific data products and integration strategies supporting AI-enabled drug discovery and development. Create scalable, interoperable, AI-ready data products connecting discovery, preclinical, clinical, safety, and real-world evidence; enable validated-biomarker data assets....Immediate start$190.8k - $300.3k
Job Description The Nonclinical Drug Safety (NDS) Therapeutic Area Leader (TAL) is a senior scientific leader responsible for advancing the vision and goals of NDS and our company as an industry leader in drug development, product registration, and post‑marketing support...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- ...environment. The role requires close collaboration with Clinical Operations, Regulatory Affairs, Biostatistics and Data Management, Drug Safety and Pharmacovigilance, Translational Medicine, Medical Affairs, and other key partner functions, as well as contribution to...
- Job Description Job Description Pharmaceutical Tooling Co Open 7am - 5:30pm Flexible 10 hour a day work schedule Overtime is about 10/hours a week and open Saturday from 7-12 looking for someone who can program from scratch using MasterCam, 3 and 4 axis mills...Work experience placementFlexible hours
$231.9k - $365k
...such as cancer, cardiometabolic diseases, eye diseases, and infectious diseases. Our Company's Research Laboratories nonclinical drug safety department at West Point, Pennsylvania site is seeking an experienced anatomic pathologist to join a highly collaborative team of...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- ...Pharmacovigilance Safety Specialist Education: Bachelor's degree or Master's degree or Advance level degree in a life science/healthcare/pharmaceutical related field. Required: Candidate is required to have at least 2 years of pharmacovigilance safety experience...For contractorsFlexible hours2 days per week
- MSD Malaysia is offering a Future Talent Program internship in Pharmacovigilance - Operations & Global Process Enablement for 10-12 weeks. You will collaborate with cross-functional global teams to enhance PV policies, contribute to AI-driven process improvements, and support...Internship
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