... profile drug and device programs. Contract role is onsite in Columbus, OH . * New 503A sterile ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
60 Propharma Group Drug Safety Associate Jobs Hiring Near You
... profile drug and device programs. Contract role is onsite in Columbus, OH . * New 503A sterile ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Qualifications Drug Safety Associate needs 2 years experience. Drug Safety Associate requires: * management of relational databases * Basic understanding of Pharmacovigilance Drug Safety Associate ...
Qualifications Drug Safety Associate needs 2 years experience. Drug Safety Associate requires: * management of relational databases * Basic understanding of Pharmacovigilance Drug Safety Associate ...
Drug Safety Associate
Parsippany, NJ · On-site
Drug Safety Associate Duration: 12 months contract, extendable up to 36 months Location: Parsippany ... You may participate in the company group medical insurance plan Safety Data Management Specialist ...
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Drug Safety Associate
Parsippany, NJ · On-site
Drug Safety Associate Duration: 12 months contract, extendable up to 36 months Location: Parsippany ... You may participate in the company group medical insurance plan Safety Data Management Specialist ...
MD required; must have previously served as Head of Pharmacovigilance / Global Drug Safety (large ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
MD required; must have previously served as Head of Pharmacovigilance / Global Drug Safety (large ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Drug Safety Associate
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 ...
Drug Safety Associate
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 ...
Drug Safety Associate
Stamford, CT · On-site
Perform coding reviews using MedDRA, WHO-DRUG, and Company Product dictionaries. * Create narrative text as required for medical orientation. * Determine follow-up requirements and request additional ...
Drug Safety Associate
Stamford, CT · On-site
Perform coding reviews using MedDRA, WHO-DRUG, and Company Product dictionaries. * Create narrative text as required for medical orientation. * Determine follow-up requirements and request additional ...
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 ...
Drug Safety Associate
Stamford, CT · On-site
Perform coding reviews using MedDRA, WHO-DRUG, and Company Product dictionaries. * Create narrative text as required for medical orientation. * Determine follow-up requirements and request additional ...
Drug Safety Associate
Stamford, CT · On-site
Perform coding reviews using MedDRA, WHO-DRUG, and Company Product dictionaries. * Create narrative text as required for medical orientation. * Determine follow-up requirements and request additional ...
Drug Safety Associate
Stamford, CT · On-site
Perform coding reviews using MedDRA, WHO-DRUG, and Company Product dictionaries. * Create narrative text as required for medical orientation. * Determine follow-up requirements and request additional ...
Drug Safety Associate
Stamford, CT · On-site
Perform coding reviews using MedDRA, WHO-DRUG, and Company Product dictionaries. * Create narrative text as required for medical orientation. * Determine follow-up requirements and request additional ...
Drug Safety Associate III
$124.50K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation ... group medical, dental and vision coverage, life and disability insurance, and flexible spending ...
Drug Safety Associate III
$124.50K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation ... group medical, dental and vision coverage, life and disability insurance, and flexible spending ...
Drug Safety Associate III
$124.50K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation ... group medical, dental and vision coverage, life and disability insurance, and flexible spending ...
Drug Safety Associate III
$124.50K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation ... group medical, dental and vision coverage, life and disability insurance, and flexible spending ...
Drug Safety Associate III
Alameda, CA · On-site
$124.50K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation ... group medical, dental and vision coverage, life and disability insurance, and flexible spending ...
Drug Safety Associate III
Alameda, CA · On-site
$124.50K - $177K/yr
This role is responsible for providing Drug Safety expertise and ensuring the quality documentation ... group medical, dental and vision coverage, life and disability insurance, and flexible spending ...
... 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 ...
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 ...
... high-profile drug and device programs. * Develop and maintain a tracking log (e.g., Excel ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
... high-profile drug and device programs. * Develop and maintain a tracking log (e.g., Excel ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
... drug and device programs. ProPharma are looking for Nurses to support clinical trials sites in ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
... drug and device programs. ProPharma are looking for Nurses to support clinical trials sites in ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
... high-profile drug and device programs. The Vice President, Nonclinical Emerging Therapies is ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
... high-profile drug and device programs. The Vice President, Nonclinical Emerging Therapies is ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Information Specialist
Western Springs, IL · On-site
... drug and device programs. Perform intake of health and safety calls, provide product safety ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Information Specialist
Western Springs, IL · On-site
... drug and device programs. Perform intake of health and safety calls, provide product safety ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
An interest in drug safety, medical information, or regulatory affairs. A proactive mindset and ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
An interest in drug safety, medical information, or regulatory affairs. A proactive mindset and ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
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 ...
ProPharma Group Jobs Information
What are the key skills and qualifications needed to thrive as a Drug Safety Associate, and why are they important?
To thrive as a Drug Safety Associate, you need a solid background in life sciences or pharmacy, knowledge of pharmacovigilance principles, and attention to detail. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and regulatory reporting systems is typically required. Strong organizational skills, effective communication, and the ability to work under deadlines help you excel in collaborating with cross-functional teams. These skills ensure accurate adverse event reporting, regulatory compliance, and protection of patient safety throughout the drug development lifecycle.
How does a Drug Safety Associate typically collaborate with other teams during the drug development process?
Drug Safety Associates regularly work in close coordination with clinical research, regulatory affairs, and medical affairs teams. They are responsible for collecting, evaluating, and reporting adverse event data, which often requires clear communication with clinical trial staff and investigators. Additionally, they may participate in cross-functional safety review meetings to discuss safety findings and ensure compliance with regulatory requirements. This collaborative environment helps ensure comprehensive safety monitoring throughout the drug's lifecycle.
What are Drug Safety Associates?
Drug Safety Associates are professionals responsible for monitoring and evaluating the safety of pharmaceutical products. They collect, analyze, and report data on adverse drug reactions to ensure compliance with regulatory requirements and to protect patient safety. Their work involves reviewing case reports, maintaining safety databases, and communicating safety information to regulatory agencies and healthcare professionals. Drug Safety Associates play a vital role in the pharmacovigilance process throughout the lifecycle of a drug.
What is the difference between Drug Safety Associate vs Pharmacovigilance Specialist?
| 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.
What other companies are hiring for Drug Safety Associate jobs?
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Full-time
Posted 28 days ago
Job description
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
Contract role is onsite in Columbus, OH.
Personnel will need to be trained in sterile compounding activities:
Providing Sterile Compounding Training. Experience in USP <797> compounding is preferred, but experience in aseptic training for 503b or aseptic drug manufacturing could be sufficient.
*Consulting/Contract opportunity lasting 4 to 6+ months
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Contract role is onsite in Columbus, OH.
- New 503A sterile compounding facility in start up mode.
- Support Training program: Beginning Dec. 1st onsite.
Personnel will need to be trained in sterile compounding activities:
- Hand hygiene, sterile garbing, gloving
- Materials Transfer
- Kitting
- Cleaning
- Weighing/Mixing
- Sterile compounding/transfer
- Filling/capping
Providing Sterile Compounding Training. Experience in USP <797> compounding is preferred, but experience in aseptic training for 503b or aseptic drug manufacturing could be sufficient.
*Consulting/Contract opportunity lasting 4 to 6+ months
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
About ProPharma Group
Sourced by ZipRecruiter
Industry
Business management consulting
Company size
51 - 200 Employees
Headquarters location
Overland Park, KS, US
Year founded
2001