Drug Safety Associate I
Horsham, PA · On-site
We deliver strategic workforce solutions that help you manage your talent and business more ... of Drug Safety usually exhibited by minimum 5 years experience in pharmaceutical safety-related ...
Horsham, PA · On-site
We deliver strategic workforce solutions that help you manage your talent and business more ... of Drug Safety usually exhibited by minimum 5 years experience in pharmaceutical safety-related ...
Horsham, PA · On-site
We deliver strategic workforce solutions that help you manage your talent and business more ... of Drug Safety usually exhibited by minimum 5 years experience in pharmaceutical safety-related ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
Drug Safety Data Management Specialist NOTE: CANDIDATES MUST HAVE ARGUS EXPERIENCE. RESPONSIBILITES: * Enter applicable information into the global safety database for initial or follow up cases ...
Drug Safety Data Management Specialist NOTE: CANDIDATES MUST HAVE ARGUS EXPERIENCE. RESPONSIBILITES: * Enter applicable information into the global safety database for initial or follow up cases ...
This role manages a multidisciplinary PV operations team, including internal PV specialists and external vendors/partners. The VP, Drug Safety also partners cross-functionally with Clinical ...
This role manages a multidisciplinary PV operations team, including internal PV specialists and external vendors/partners. The VP, Drug Safety also partners cross-functionally with Clinical ...
Boston, MA · On-site
$105K - $115K/yr
Monitoring of ICSRs in workflow and managing processing timelines * As needed, support data ... Proficiency in MedDRA and WHO Drug dictionaries. * Experience with Veeva safety database, EDC ...
Boston, MA · On-site
$105K - $115K/yr
Monitoring of ICSRs in workflow and managing processing timelines * As needed, support data ... Proficiency in MedDRA and WHO Drug dictionaries. * Experience with Veeva safety database, EDC ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
Drug Safety Public Health Coordinator Duration: 6 Months Location: Foster City, CA 94404 * Sets ... Maintain and manage dept. Safety mailbox, distributing to relevant parties as applicable. * May ...
Drug Safety Public Health Coordinator Duration: 6 Months Location: Foster City, CA 94404 * Sets ... Maintain and manage dept. Safety mailbox, distributing to relevant parties as applicable. * May ...
Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist Be a part of a global team that ... This role is responsible for leading safety signal detection and management, aggregate safety ...
Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist Be a part of a global team that ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and ... This role is responsible for leading safety signal detection and management, aggregate safety ...
San Diego, CA · On-site
$180 - $280/hr
Lead safety signal management activities and oversight of vendor delegated to conduct signal ... Minimum 10+ years of experience in Drug Safety/Pharmacovigilance for a biotech/pharmaceutical ...
San Diego, CA · On-site
$180 - $280/hr
Lead safety signal management activities and oversight of vendor delegated to conduct signal ... Minimum 10+ years of experience in Drug Safety/Pharmacovigilance for a biotech/pharmaceutical ...
The Drug Safety Associate I will support ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B and FDA/EMA ...
Quick apply
The Drug Safety Associate I will support ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B and FDA/EMA ...
Miami, FL · On-site
This role manages a multidisciplinary PV operations team, including internal PV specialists and external vendors/partners. The VP, Drug Safety also partners cross-functionally with Clinical ...
Miami, FL · On-site
This role manages a multidisciplinary PV operations team, including internal PV specialists and external vendors/partners. The VP, Drug Safety also partners cross-functionally with Clinical ...
Our client is looking for Drug Safety Data Management Specialist - with the Argus experience! RESPONSIBILITIES: Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event ...
Our client is looking for Drug Safety Data Management Specialist - with the Argus experience! RESPONSIBILITIES: Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event ...
California, MO · On-site
$150 - $190/hr
The primary responsibilities are to manage safety contract service organizations (CSOs) with >=95 ... Requires at least 12 years of drug safety and pharmacovigilance experience (post-market safety ...
California, MO · On-site
$150 - $190/hr
The primary responsibilities are to manage safety contract service organizations (CSOs) with >=95 ... Requires at least 12 years of drug safety and pharmacovigilance experience (post-market safety ...
Princeton, NJ · On-site
$235K - $353K/yr
You will work together with other Drug Safety staff in managing the safety assessment of products, including review of individual and aggregate AEs and the scientific literature, preparing safety ...
Princeton, NJ · On-site
$235K - $353K/yr
You will work together with other Drug Safety staff in managing the safety assessment of products, including review of individual and aggregate AEs and the scientific literature, preparing safety ...
You will work together with other Drug Safety staff in managing the safety assessment of products, including review of individual and aggregate AEs and the scientific literature, preparing safety ...
You will work together with other Drug Safety staff in managing the safety assessment of products, including review of individual and aggregate AEs and the scientific literature, preparing safety ...
$37K - $46K
3% of jobs
$46K - $55.1K
6% of jobs
$55.1K - $64.1K
12% of jobs
$66.4K is the 25th percentile. Wages below this are outliers.
$64.1K - $73.2K
16% of jobs
The median wage is $80.2K / yr.
$73.2K - $82.2K
17% of jobs
$82.2K - $91.3K
13% of jobs
$98.7K is the 75th percentile. Wages above this are outliers.
$91.3K - $100.3K
11% of jobs
$100.3K - $109.4K
8% of jobs
$109.4K - $118.4K
7% of jobs
$118.4K - $127.5K
4% of jobs
$127.5K - $136.5K
3% of jobs
$37K
$86K
$136.5K
| Aspect | Drug Safety Manager | Pharmacovigilance Specialist |
|---|---|---|
| Credentials | Typically requires a degree in pharmacy, life sciences, or related field; certifications like PV or REMS are common | Similar educational background; often holds certifications in pharmacovigilance or drug safety |
| Work Environment | Leads drug safety teams, manages safety data, and oversees compliance within pharmaceutical companies | Focuses on collecting, analyzing, and reporting safety data, often working under supervision |
| Industry Usage | Used in pharmaceutical and biotech companies for overseeing safety programs | Commonly used in regulatory agencies and contract research organizations |
While both roles involve drug safety and require similar qualifications, the Drug Safety Manager typically has a leadership role overseeing safety operations, whereas the Pharmacovigilance Specialist focuses on data collection and analysis. The manager has broader responsibilities, including team management and strategic planning.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
Responsible for the receipt and data entry of adverse event reports following company standard operating procedures, internal business practices and regulatory guidance documents, to ensure compliance with worldwide safety regulations and corporate policies.
PRINCIPAL RESPONSIBILITIES:
Case processing: 95%
Definition: The completion of full case information on the database, including quality review to ensure accuracy and completeness
Activities Include:
May Triage and classify ICSRs for report type, seriousness, causality, expectedness/labeling and reporting; prioritize ICSR according to regulatory requirements
Confirmation of Safety Coordinator case registry data
Database searches as necessary
Completion of remaining case data entry, including narrative or auto-narrative
Completion of risk and quality (label, approval, manual coding and quality review steps).
Clarification of unclear or illegible information from the LSO or Call Centre
Discussion of source documents, coding conventions and ad-hoc queries with Pharmacovigilance Physician
Request deletions as necessary
Single case unblinding
Processes & Procedures:
Definition: Continuing awareness of company procedures and guidelines to maintain regulatory compliance
Activities Include:
Standard Operating Procedures and Working Instructions
Department guidance documents
MedDRA coding dictionary and MedDRA Points to Consider
Understand relevant safety implications regarding contracts with operating companies and/or marketing partners
DECISION-MAKING AND PROBLEM-SOLVING:
Application and knowledge of Departmental processes and guidelines, regulations and regulatory guidelines, contractual arrangements, product specific information and database/systems functionality to individual case processing and evaluation. Communicate questions clearly and concisely to the appropriate audience and accompany with possible solutions.
REPORTING RELATIONSHIPS: Describe where this position fits in relation to the rest of the department it resides.
Supervised by Senior DSA
WORKING RELATIONSHIPS/INTERFACES: Describe the primary working relationships (internal & external) and primary interfaces along with the frequency and purpose/nature.
Global Medical Safety Operations (GMSO) is a functional area within the Global Medical Organization (GMO)
All others in GMSO
Medical Affairs
Clinical Affairs
Contract Research Organizations
Local Safety Officers
Marketing Partners
EDUCATION & EXPERIENCE REQUIREMENTS: Describe the minimum knowledge, skill and ability requirements for the position. Include any degrees or certifications which are required and/or desirable.
Registered Nurse OR
Health/Biomedical Degree (BS, PhD or other related scientific degree/qualification) OR
Licensed Practical Nurse without Bachelors degree but with knowledge of Drug Safety usually exhibited by minimum 5 years experience in pharmaceutical safety-related role.
Pharmaceutical industry experience is preferred
Required Skills/Abilities
Intermediate Information Technology Skills
Data entry experience desired
Accountability for delivery of results
Decision making skills
Problem solving skills
Proactive approach/uses own initiative
Manages owe work, able to prioritize, plan and organize work assignments and work under strict timelines
Ability to follow guidelines, working practices etc. Experience of working with SOP/WI preferred
Quality oriented, with attention to detail/accuracy
Flexibility/Adaptability
Positive attitude
Good team player
Ability to work independently and to collaborate
Good written and verbal communication skills
Understanding of medical terminology
Ability to summarize medical information
Thanks!!
With Regards,
Sasha Sharma
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Direct: 732-662-7964 | (W) 732-549-2030 x 219
Inc. 5000 - 2007-2015 (9 Years in a row)
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996