... 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 ...
Quick apply
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 ...
Drug Safety Associate
San Diego, CA · On-site
$77K - $90K/yr
The Drug Safety Associate provides operational and documentation support for the company's clinical safety and pharmacovigilance activities. Working closely with the Drug Safety Manager, this role ...
Drug Safety Associate
San Diego, CA · On-site
$77K - $90K/yr
The Drug Safety Associate provides operational and documentation support for the company's clinical safety and pharmacovigilance activities. Working closely with the Drug Safety Manager, this role ...
Drug Safety Associate
Pennington, NJ · On-site
$110K - $120K/yr
... Group. • Maintain Adverse event and safety database log and coordinate distribution of safety ... for other Drug Safety Associate's cases. • Assist with additional drug safety activities as ...
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Drug Safety Associate
Pennington, NJ · On-site
$110K - $120K/yr
... Group. • Maintain Adverse event and safety database log and coordinate distribution of safety ... for other Drug Safety Associate's cases. • Assist with additional drug safety activities as ...
Drug Safety Associate
$77K - $90K/yr
Description The Drug Safety Associate provides operational and documentation support for the company's clinical safety and pharmacovigilance activities. Working closely with the Drug Safety Manager ...
Drug Safety Associate
$77K - $90K/yr
Description The Drug Safety Associate provides operational and documentation support for the company's clinical safety and pharmacovigilance activities. Working closely with the Drug Safety Manager ...
Drug Safety Associate
San Diego, CA · On-site
$77K - $90K/yr
The Drug Safety Associate provides operational and documentation support for the company's clinical safety and pharmacovigilance activities. Working closely with the Drug Safety Manager, this role ...
Quick apply
Drug Safety Associate
San Diego, CA · On-site
$77K - $90K/yr
The Drug Safety Associate provides operational and documentation support for the company's clinical safety and pharmacovigilance activities. Working closely with the Drug Safety Manager, this role ...
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 ...
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 II
Norwood, MA · On-site
The Drug Safety Associate II/Senior Drug Safety Associate is the senior technical contributor anchoring Corbus Pharmaceuticals' in-house PV function. In addition to managing complex ICSRs and SUSARs ...
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Drug Safety Associate II
Norwood, MA · On-site
The Drug Safety Associate II/Senior Drug Safety Associate is the senior technical contributor anchoring Corbus Pharmaceuticals' in-house PV function. In addition to managing complex ICSRs and SUSARs ...
Drug Safety Associate
Cambridge, MA · On-site
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
Cambridge, MA · On-site
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
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 I
Norwood, MA · On-site
The Drug Safety Associate I will serve as the primary ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B ...
Quick apply
Drug Safety Associate I
Norwood, MA · On-site
The Drug Safety Associate I will serve as the primary ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B ...
Drug Safety Associate I
Norwood, MA · Hybrid
The Drug Safety Associate I will serve as the primary ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B ...
Drug Safety Associate I
Norwood, MA · Hybrid
The Drug Safety Associate I will serve as the primary ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B ...
Drug Safety Associate I
Norwood, MA · On-site
The Drug Safety Associate I will serve as the primary ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B ...
Drug Safety Associate I
Norwood, MA · On-site
The Drug Safety Associate I will serve as the primary ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B ...
Sr. Drug Safety Associate
Cambridge, MA · On-site
... Associate will provide partner / vendor oversight in relation to Clinical Trial safety report ... drug safety/Pharmacovigilance in pharmaceutical industry setting or the equivalent Experience ...
Sr. Drug Safety Associate
Cambridge, MA · On-site
... 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 ...
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 ...
... 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 ...
... 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 ...
Facilities Inventory Control Clerk (Contract, Onsite - NY)
Western Springs, IL · On-site
$17 - $20.50/hr
... profile drug and device programs. Facilities Inventory Associate- Rensselaer, NY Duration: 12 ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
Facilities Inventory Control Clerk (Contract, Onsite - NY)
Western Springs, IL · On-site
$17 - $20.50/hr
... profile drug and device programs. Facilities Inventory Associate- Rensselaer, NY Duration: 12 ... ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone ...
ProPharma Group Jobs Information
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Full-time
Posted 27 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