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Drug Safety And Medical Information Specialist Jobs

Drug Safety Specialist Jobs
By Integrated Resources, Inc ( IRI ) At Pennsylvania, United States

• Monitor group mailboxes utilized for the centralization of process/subject specific inquiries.

Drug Safety Associate Jobs
By GForce Life Sciences At San Francisco, CA, United States
Supports all study management-related activities
Demonstrates expertise in computer skills and database experience (i.e Microsoft Office Suite and Google Applications )
Familiarity with project management software tools, methodologies, and best practices
Benefits - Medical, Dental, Vision
Perform Individual Case Safety Reports (ICSR) Activities
Performs Outbound Submission and Tracking (OST) for literature ICSRs and submits relevant documentation to the health authority
Medical Information Specialist Jobs
By Randstad USA At United States
Manage Medical Information email mailbox and perform data entry of requests into IRMS
Understand and comply with literature copyright requirements
Minimum of 2-3 years of experience in a drug information, medical information, or pharmaceutical call center
Infectious Diseases specialty training or experience is desirable
Excellent verbal, written, and telephone communication skills
Knowledge of medical terminology, pathophysiology, pharmacology, pharmacotherapeutics, and laboratory diagnostic tests specifically in infectious disease
Medical Safety Specialist Jobs
By Akkodis At United States
Remote Medical Safety Specialist (MSS) job responsibilities include:
• Maintain knowledge of relevant regulations for classifying and reporting medical device and drug adverse events.
• Ability to make clinical decisions and formulate appropriate queries based on sound medical knowledge.
• Ability to follow national and international regulations and reporting requirement for adverse events, medical device complaints.
• Strong organization, prioritization skills and attention to detail.
Pay/Salary Range: $50.00 to $55.00 per hour.
Drug Safety Specialist Jobs
By Roth Staffing At Princeton, NJ, United States
Preferred 5 years of Drug Safety & PV relevant experience and strong knowledge of PV practices
Excellent written and verbal communication skills in English
Working knowledge of Excel, Power Point and Word
Support Pharmacovigilance (PV) Quality & Compliance activities
Support development and maintenance of PV process documents (e.g., SOPs, WIs)
Support activities related to PV audits and inspections
Drug Safety Specialist Jobs
By Roth Staffing At San Diego, CA, United States
Preferred 5 years of Drug Safety & PV relevant experience and strong knowledge of PV practices
Excellent written and verbal communication skills in English
Working knowledge of Excel, Power Point and Word
Support Pharmacovigilance (PV) Quality & Compliance activities
Support development and maintenance of PV process documents (e.g., SOPs, WIs)
Support activities related to PV audits and inspections
Medical Information Specialist Jobs
By Integrated Resources, Inc ( IRI ) At South San Francisco, CA, United States
Medical literature surveillance and evaluation skills.
Previous relevant industry work experience, including Scientific Communications.
Complete all assigned work on time, on-target and with the highest levels of clinical accuracy and relevance.
Take on and complete departmental projects as assigned.
Act in complete compliance with all laws, regulations, and policies.
Utilize only approved resources and processes to meet goals and targets.
Drug Safety Specialist (Remote)
By Tandym Group At Boston, MA, United States
Solid problem solving and time management skills
In-depth knowledge of EU safety regulation and compliance
Prior experience writing SOPs, editing/reviewing SOPS, EU experience a must, Audit experience very important
Excellent communication skills (written and verbal)
The qualified professional in this role will be working 20 to 30 hours a week.***
Focus on bone studies and bone loss (osteoporotic fractures)
Medical Information Specialist Jobs
By Revance At Nashville, TN, United States
Experience using Customer Relationship Management (CRM )systems
Document the medical inquiries and fulfillment accurately within the Customer Relationship Management (CRM) system
Excellent communication skills, both written and oral
Working knowledge of drug development, regulatory approval processes, clinical trial methodologies, and guidelines
Team oriented with excellent interpersonal skills and ability to develop and maintain effective professional relationships
1-3 years of medical information or medical affairs experience in a life science, pharmaceutical, or medical device company
Medical Information Specialist Jobs
By Mindlance At Princeton, NJ, United States
The Medical Information Contractor’s responsibilities will include the following:
• Limits corporate liability by meeting the medical ethical and legal responsibilities of providing product/device related information
• Serves as an educational resource to both internal and external customers
• 1-3 years’ experience with providing medical information to customers
• Excellent interpersonal, communication and negotiation skills.
• MS Office; Experience with MI Systems a plus, but not required
Drug Safety Associate Jobs
By SPECTRAFORCE At North Chicago, IL, United States
Demonstrates ability to lead project work. Proven success in results-driven process management
Supporting implementation of strategies to enhance PDI excellence in providing the highest level of customer experience.
Other duties may be assigned based on the need or work requirement of the organization.
2-4 years clinical healthcare and previous pharmaceutical industry experience. Pharmaceutical industry contact center experience preferred.
Demonstrates strong attention to detail and problem-solving skills
Core knowledge of Industry regulations (ICH, FDA, EMEA, MHRA)
Drug Safety Specialist-Contractor Jobs
By Halozyme Therapeutics, Inc. At , , Nj $45 - $55 an hour
Excellent knowledge of FDA safety reporting requirements
Perform data entry of post-marketing and clinical ICSRs into the safety database
Manage the drug safety mailbox
Identify and respond appropriately to new safety reports to protect patients and maintain full compliance with regulatory requirements
Bachelor’s degree in a life science required with at least 2 years drug safety experience
Experience with the content of pharmacovigilance documents such as SOPs, guidelines, safety plans
Drug Safety Specialist Jobs
By SynapOne At Thousand Oaks, CA, United States
Preferred Educational Qualification for the role:
Preferred experience for the role:
Complete data entry in database
Perform calls to customer for obtaining detailed information significant for the scientific evaluation of the case
Perform follow up calls as per the SOP
Contribute to the development and implementation of new safety-related systems, processes and procedures within the process.
Drug Safety Associate Jobs
By ICON At , Remote
Services rendered will adhere to applicable Johnson & Johnson SOPs, WIs, policies, local regulatory requirements, etc.
Operational support for SUSAR/SUSAR LL/DSUR case distribution via safety reporting systems according to the Global Safety Reporting´s current processes.
Reconciliation with safety partners and compliance analysis
Support changes to departmental documentation as needed.
Communication with the service users and all involved partners
Support CAPA investigations and or action plans as needed.
Drug Safety Specialist Jobs
By Hydrogen Group At California, United States
Excellent knowledge of FDA safety reporting requirements.
Knowledge of other software required: Oracle Argus – End User-level experience.
Bachelor’s degree in a life science required with at least 2 years drug safety experience.
Experience with Argus and workflows.
Experience with the content of pharmacovigilance documents such as SOPs, guidelines, safety plans.
Software Knowledge: Argus, Windows, MS Office (Outlook, Word, Excel).
Medical Information Specialist Jobs
By Integrated Resources, Inc ( IRI ) At Pennsylvania, United States
Education: Bachelor’s degree or above in a scientific field.
• Min 2 years medical writing experience; previous work experience in a global medical information group, preferred.
• Strong writing, verbal and interpersonal communication skills.
• Ideal candidate should have proficiency with MS Office, PowerPoint, EndNote; Veeva Vault MedComms experience is preferred.
• Effective literature searching, fact-checking, and data summarization skills.
• Knowledge of Vaccine and Infectious Diseases/Products.
Contract Role-Manager Drug Safety
By Jobot At Fort Lauderdale, FL, United States
Experience with safety data management and signal detection
Experience in project management and clinical operations
Experience in preparing and presenting safety reports to senior management and regulatory agencies.
Act as record management coordinator for the Drug Safety Team
Manage CRO relationships and ensure timely delivery of safety data
3+ years of experience in drug safety and pharmacovigilance
Contract Role-Manager Drug Safety
By Jobot At New York, NY, United States
Experience with safety data management and signal detection
Experience in project management and clinical operations
Experience in preparing and presenting safety reports to senior management and regulatory agencies.
Act as record management coordinator for the Drug Safety Team
Manage CRO relationships and ensure timely delivery of safety data
3+ years of experience in drug safety and pharmacovigilance
Drug Safety Specialist Jobs
By Denrose Search Group At Morristown, NJ, United States
• Knowledge of clinical trial activities Requirements and personal skills
• 5-7 years of experience in a pharmacovigilance role •
• Excellent verbal and written communication skills, ability to convey moderately complex technical information clearly to others
• Sound knowledge of Microsoft Office applications
• Uncommon flexibility and ability to manage simultaneous priorities, changing deadlines, and limited resources
High level of technical proficiency with computer systems and software o
Usa - Medical Information And Review Manager
By Takeda Pharmaceutical At , Lexington, Ma
1-2 years of healthcare or related experience (managed markets, clinical practice, research or academic) following award of doctoral degree.
Possesses good communication skills, both oral and written, and able to engender trust and respect of peers, subordinates and superiors.
Clinical, research, or teaching experience.
Board Certification in therapeutic area of interest.
Travel may vary depending on therapeutic responsibilities.
Formulate medical responses and recommendations (including errata) as requested by scientific journals and organizations.

Are you looking for a challenging and rewarding role in the medical field? We are looking for a Drug Safety and Medical Information Specialist to join our team! As a Drug Safety and Medical Information Specialist, you will be responsible for providing accurate and timely medical information to healthcare professionals and patients. You will also be responsible for monitoring drug safety data and providing reports to the appropriate regulatory agencies. If you have a passion for helping others and a desire to make a difference in the medical field, this is the perfect job for you!

Overview Drug Safety and Medical Information Specialists are responsible for providing medical and safety information to healthcare professionals and patients. They are responsible for collecting and analyzing data related to drug safety and medical information, and for providing advice and guidance to healthcare professionals and patients. Detailed Job Description Drug Safety and Medical Information Specialists are responsible for collecting and analyzing data related to drug safety and medical information. They must be knowledgeable about the latest developments in the field of drug safety and medical information, and must be able to interpret and communicate this information to healthcare professionals and patients. They must be able to identify potential safety issues and provide advice and guidance to healthcare professionals and patients. They must also be able to provide accurate and timely medical information to healthcare professionals and patients. Job Skills Required
• Knowledge of drug safety and medical information
• Ability to interpret and communicate medical and safety information
• Ability to identify potential safety issues
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to work under pressure
• Excellent organizational and time management skills
• Ability to use computer software programs
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in a medical or healthcare setting
• Certification in drug safety and medical information
Job Knowledge
• Knowledge of drug safety and medical information
• Knowledge of medical terminology
• Knowledge of healthcare regulations and standards
• Knowledge of computer software programs
Job Experience
• Previous experience in a medical or healthcare setting
• Previous experience in a drug safety and medical information role
Job Responsibilities
• Collect and analyze data related to drug safety and medical information
• Provide accurate and timely medical information to healthcare professionals and patients
• Identify potential safety issues and provide advice and guidance to healthcare professionals and patients
• Monitor and report on drug safety and medical information
• Develop and implement strategies to improve drug safety and medical information
• Maintain records and databases related to drug safety and medical information
• Participate in research projects related to drug safety and medical information