Peapack, NJ · On-site
$21/hr
Qualifications Drug Safety Associate needs 2 years experience. Drug Safety Associate requires: * management of relational databases * Basic understanding of Pharmacovigilance Drug Safety Associate ...
Peapack, NJ · On-site
$21/hr
Qualifications Drug Safety Associate needs 2 years experience. Drug Safety Associate requires: * management of relational databases * Basic understanding of Pharmacovigilance Drug Safety Associate ...
Parsippany, NJ · On-site
Drug Safety Associate Duration: 12 months contract, extendable up to 36 months Location: Parsippany, NJ Note: The client has the right-to-hire you as a permanent employee at any time during or after ...
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Parsippany, NJ · On-site
Drug Safety Associate Duration: 12 months contract, extendable up to 36 months Location: Parsippany, NJ Note: The client has the right-to-hire you as a permanent employee at any time during or after ...
Boulder, CO · On-site
The Safety Associate works fairly independently in receiving and reviewing serious adverse event (SAE) reports for completeness, performing initial triage, data entry into the Safety database and ...
Boulder, CO · On-site
The Safety Associate works fairly independently in receiving and reviewing serious adverse event (SAE) reports for completeness, performing initial triage, data entry into the Safety database and ...
Boulder, CO · On-site
The Safety Associate works fairly independently in receiving and reviewing serious adverse event (SAE) reports for completeness, performing initial triage, data entry into the Safety database and ...
Boulder, CO · On-site
The Safety Associate works fairly independently in receiving and reviewing serious adverse event (SAE) reports for completeness, performing initial triage, data entry into the Safety database and ...
Title: Senior Safety Associate (Global Case Management) Location: Cambridge, MA Duration: 8 - 12 Months+ Job Summary The Safety and Benefit Risk, Global Case Management department performs ...
Title: Senior Safety Associate (Global Case Management) Location: Cambridge, MA Duration: 8 - 12 Months+ Job Summary The Safety and Benefit Risk, Global Case Management department performs ...
OR · On-site
As a Patient Safety Associate I, you'll play a vital role in supporting drug safety, clinical trials, and postmarketing surveillance activities in post-market surveillance, with some exposure to ...
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
Alameda, CA · On-site
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
Alameda, CA · On-site
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
Alameda, CA · On-site
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
Alameda, CA · On-site
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
$124K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs). This role provides support for all ...
... Associate will provide partner / vendor oversight in relation to Clinical Trial safety report ... drug safety/Pharmacovigilance in pharmaceutical industry setting or the equivalent Experience ...
... Associate will provide partner / vendor oversight in relation to Clinical Trial safety report ... drug safety/Pharmacovigilance in pharmaceutical industry setting or the equivalent Experience ...
As a Patient Safety Associate I , you'll play a vital role in supporting drug safety, clinical trials, and post-marketing surveillance activities in post-market surveillance, with some exposure to ...
As a Patient Safety Associate I , you'll play a vital role in supporting drug safety, clinical trials, and post-marketing surveillance activities in post-market surveillance, with some exposure to ...
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 ...
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 ...
Signal Detection/Drug Safety Associate II Job Location: Bridgewater, NJ Client -Sanofi (5822901) Duties: Please note: The Job Title is Signal Detection and Management Associate Primary ...
Signal Detection/Drug Safety Associate II Job Location: Bridgewater, NJ Client -Sanofi (5822901) Duties: Please note: The Job Title is Signal Detection and Management Associate Primary ...
Drug Safety Operations Associate LOCATION: Stamford, CT DURATION: 12 months * Position performs adverse event processing and submission responsibilities supporting the Case Management function within ...
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Drug Safety Operations Associate LOCATION: Stamford, CT DURATION: 12 months * Position performs adverse event processing and submission responsibilities supporting the Case Management function within ...
To facilitate operational integration and alignment with US Drug Safety Medicine and providing ... Associate Medical Directors to ensure alignment by providing operational expertise. - Represent ...
To facilitate operational integration and alignment with US Drug Safety Medicine and providing ... Associate Medical Directors to ensure alignment by providing operational expertise. - Represent ...
Marlborough, MA · On-site
$80/hr
Qualifications Drug Safety Specialist needs 5-7 years in Cognos report development and project management, preferably within the pharmaceutical industry. Drug Safety Specialist requires:
Marlborough, MA · On-site
$80/hr
Qualifications Drug Safety Specialist needs 5-7 years in Cognos report development and project management, preferably within the pharmaceutical industry. Drug Safety Specialist requires:
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 ...
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 ...
What the Senior Drug Safety, Pharmacovigilance does at Worldwide Responsible for the collection ... Independently serves as Lead PV Associate on large sized studies/programs that are moderate to ...
What the Senior Drug Safety, Pharmacovigilance does at Worldwide Responsible for the collection ... Independently serves as Lead PV Associate on large sized studies/programs that are moderate to ...
$12.26 - $18.95
7% of jobs
$18.95 - $25.63
4% of jobs
$25.63 - $32.32
3% of jobs
$38.25 is the 25th percentile. Wages below this are outliers.
$32.32 - $39.01
12% of jobs
The median wage is $44.20 / hr.
$39.01 - $45.69
31% of jobs
$45.69 - $52.38
15% of jobs
$54.36 is the 75th percentile. Wages above this are outliers.
$52.38 - $59.07
12% of jobs
$59.07 - $65.76
0% of jobs
$65.76 - $72.44
9% of jobs
$72.44 - $79.13
5% of jobs
$79.13 - $85.82
2% of jobs
$12
$49
$85
A drug safety associate works in the medical industry to monitor the safety of pharmaceutical drugs and to evaluate and prevent adverse reactions in patients. A career in drug safety, also called pharmacovigilance, can include work with clinical research organizations that conduct trials, biotechnology firms, pharmaceutical companies, or government agencies like the National Institutes of Health (NIH). Drug safety associates need excellent research skills, a strong background in medical or biological science, and in-depth knowledge of the Food and Drug Administration (FDA) regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether specific pharmaceutical drugs are safe.
| Aspect | Drug Safety Associate | Pharmacovigilance Specialist |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or healthcare, with certifications like PV or drug safety training | Similar credentials, often with additional certifications or experience in pharmacovigilance |
| Work Environment | Pharmaceutical companies, CROs, or healthcare settings focusing on safety data management | Same as Drug Safety Associate, often with more specialized pharmacovigilance tasks |
| Employer & Industry | Pharmaceutical, biotech, and healthcare industries | Same industries, with a focus on drug safety monitoring and compliance |
Both roles involve monitoring drug safety data, reporting adverse events, and ensuring regulatory compliance. The main difference lies in the scope and specialization, with Pharmacovigilance Specialists often handling more complex safety data analysis and regulatory submissions. However, the roles overlap significantly, and job titles are sometimes used interchangeably depending on the organization.
$21/hr
Contractor
Posted 10 days ago
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.
Drug Safety Associate needs 2 years experience.
Drug Safety Associate requires:
Drug Safety Associate duties are:
$21/hr
12 months+
Sourced by ZipRecruiter
Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.
Recruiting and staffing services
11 - 50 Employees
Austell, GA, US
2009
