Knowledgeable about PhRMA, OIG and other industry regulations and guidelines as appropriate. Primary Role Provide a brief summary Summarize key areas of accountability and budget responsibility ...
Knowledgeable about PhRMA, OIG and other industry regulations and guidelines as appropriate. Primary Role Provide a brief summary Summarize key areas of accountability and budget responsibility ...
Medical Science Liaison, Florida
OR · Remote
Within PhRMA guidelines, supports company-sponsored research, investigator-initiated research, and publications. * Supports planning and execution of advisory boards * Stays abreast of emerging ...
Medical Science Liaison, Florida
OR · Remote
Within PhRMA guidelines, supports company-sponsored research, investigator-initiated research, and publications. * Supports planning and execution of advisory boards * Stays abreast of emerging ...
This role ensures compliance with PhRMA Code, internal policies, and all applicable regulations while supporting the generation and communication of scientific insights that inform Medical Affairs ...
This role ensures compliance with PhRMA Code, internal policies, and all applicable regulations while supporting the generation and communication of scientific insights that inform Medical Affairs ...
This role ensures compliance with PhRMA Code, internal policies, and all applicable regulations while supporting the generation and communication of scientific insights that inform Medical Affairs ...
This role ensures compliance with PhRMA Code, internal policies, and all applicable regulations while supporting the generation and communication of scientific insights that inform Medical Affairs ...
Scientist II, Specialty Formulations R&D
Denville, NJ · On-site
$80K - $85K/yr
To apply, visit RiconPharma LLC's, Ingenus Phrma affil., wbsite @ & apply by email your CV to hr@ingenus.com. Ref # 62026
Scientist II, Specialty Formulations R&D
Denville, NJ · On-site
$80K - $85K/yr
To apply, visit RiconPharma LLC's, Ingenus Phrma affil., wbsite @ & apply by email your CV to hr@ingenus.com. Ref # 62026
Senior Counsel - Compliance
$262K - $295K/yr
Provide guidance regarding the Anti-Kickback Statute, False Claims Act, Sunshine Act, FDA requirements, PhRMA Code, and applicable state healthcare compliance laws * Develop and oversee compliance ...
Senior Counsel - Compliance
$262K - $295K/yr
Provide guidance regarding the Anti-Kickback Statute, False Claims Act, Sunshine Act, FDA requirements, PhRMA Code, and applicable state healthcare compliance laws * Develop and oversee compliance ...
Senior Counsel - Compliance
OR · Remote
$262K - $295K/yr
Provide guidance regarding the Anti-Kickback Statute, False Claims Act, Sunshine Act, FDA requirements, PhRMA Code, and applicable state healthcare compliance laws * Develop and oversee compliance ...
Senior Counsel - Compliance
OR · Remote
$262K - $295K/yr
Provide guidance regarding the Anti-Kickback Statute, False Claims Act, Sunshine Act, FDA requirements, PhRMA Code, and applicable state healthcare compliance laws * Develop and oversee compliance ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. QualificationsQualifications: * Bachelor's degree required; advanced degree preferred ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. QualificationsQualifications: * Bachelor's degree required; advanced degree preferred ...
Associate Director, Medical Information and Review
Waltham, MA · On-site
$167K - $230K/yr
Ensure all medical information activities comply with applicable laws, regulations, and industry standards (e.g., PhRMA, FDA, EMA) * Participate in internal audits and regulatory health authority ...
Associate Director, Medical Information and Review
Waltham, MA · On-site
$167K - $230K/yr
Ensure all medical information activities comply with applicable laws, regulations, and industry standards (e.g., PhRMA, FDA, EMA) * Participate in internal audits and regulatory health authority ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications: * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications: * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Understanding of FDA/PhRMA promotional guidelines and compliance standards. Preferred: * Experience in buy-and-bill environments, rebate tiering, and ASP reimbursement structures. * Experience with ...
Understanding of FDA/PhRMA promotional guidelines and compliance standards. Preferred: * Experience in buy-and-bill environments, rebate tiering, and ASP reimbursement structures. * Experience with ...
Understanding of FDA/PhRMA promotional guidelines and compliance standards. Preferred: * Experience in buy-and-bill environments, rebate tiering, and ASP reimbursement structures. * Experience with ...
Understanding of FDA/PhRMA promotional guidelines and compliance standards. Preferred: * Experience in buy-and-bill environments, rebate tiering, and ASP reimbursement structures. * Experience with ...
Senior Director, Healthcare Compliance
$141K - $189K/yr
Health & Human Services Office of Inspector General (OIG) Compliance Program Guidance, PhRMA Code Standout Skills for Impact: * Maintain deep expertise in applicable laws and monitor external ...
Senior Director, Healthcare Compliance
$141K - $189K/yr
Health & Human Services Office of Inspector General (OIG) Compliance Program Guidance, PhRMA Code Standout Skills for Impact: * Maintain deep expertise in applicable laws and monitor external ...
Associate Director, Medical Information and Review
Waltham, MA · On-site
$167K - $230K/yr
Ensure all medical information activities comply with applicable laws, regulations, and industry standards (e.g., PhRMA, FDA, EMA) * Participate in internal audits and regulatory health authority ...
Associate Director, Medical Information and Review
Waltham, MA · On-site
$167K - $230K/yr
Ensure all medical information activities comply with applicable laws, regulations, and industry standards (e.g., PhRMA, FDA, EMA) * Participate in internal audits and regulatory health authority ...
Work with the Compliance Steering Committee to govern, document, and measure the development and execution of all US Commercial organization training on corporate policies, procedures, PhRMA ...
New
Quick apply
Work with the Compliance Steering Committee to govern, document, and measure the development and execution of all US Commercial organization training on corporate policies, procedures, PhRMA ...
New
Understanding of FDA/PhRMA promotional guidelines and compliance standards. Preferred: * Experience in buy-and-bill environments, rebate tiering, and ASP reimbursement structures. * Experience with ...
Understanding of FDA/PhRMA promotional guidelines and compliance standards. Preferred: * Experience in buy-and-bill environments, rebate tiering, and ASP reimbursement structures. * Experience with ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications: * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. Qualifications: * Bachelor's degree required; advanced degree preferred. * 5-7 years ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. QualificationsQualifications: * Bachelor's degree required; advanced degree preferred ...
Execute all responsibilities in compliance with company policies, FDA/PhRMA guidelines, and industry standards. QualificationsQualifications: * Bachelor's degree required; advanced degree preferred ...
Phrma information
See salary details
$8.89 - $13.70
16% of jobs
$15.17 is the 25th percentile. Wages below this are outliers.
$13.70 - $18.51
29% of jobs
The median wage is $19.71 / hr.
$18.51 - $23.32
19% of jobs
$27.58 is the 75th percentile. Wages above this are outliers.
$23.32 - $28.13
12% of jobs
$28.13 - $32.93
8% of jobs
$32.93 - $37.74
5% of jobs
$37.74 - $42.55
4% of jobs
$42.55 - $47.36
2% of jobs
$47.36 - $52.16
2% of jobs
$52.16 - $56.97
1% of jobs
$56.97 - $61.78
1% of jobs
$8
$26
$61
How much do phrma jobs pay per hour?
As of Jul 25, 2026, the average hourly pay for phrma in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.
What types of cross-functional collaboration can I expect as a professional in the pharmaceutical industry (PhRMA)?
Working in the pharmaceutical industry often involves significant collaboration with a variety of teams, including research and development, regulatory affairs, marketing, and medical affairs. You will likely participate in multidisciplinary meetings to align on product strategy, compliance, and timelines. Effective communication and teamwork are essential as you contribute to bringing new therapies to market while ensuring all regulatory and quality standards are met. This collaborative environment not only enhances your professional network but also provides opportunities to learn from experts in different fields.
What are the key skills and qualifications needed to thrive as a pharmaceutical industry professional, and why are they important?
To thrive in the pharmaceutical industry, you typically need a background in life sciences or pharmacy, strong analytical skills, and knowledge of drug development and regulatory processes. Familiarity with laboratory information management systems (LIMS), statistical analysis software, and relevant certifications such as Good Manufacturing Practice (GMP) are commonly required. Excellent communication, teamwork, and problem-solving abilities are vital soft skills in this sector. These competencies ensure safe, effective product development and regulatory compliance in a highly regulated and collaborative environment.
What is PhRMA?
PhRMA stands for the Pharmaceutical Research and Manufacturers of America. It is a trade association that represents leading biopharmaceutical research companies in the United States. PhRMA advocates for policies that support the discovery of new medicines by its member companies, promote patient access to medications, and foster medical innovation. The organization also provides information about the value of biopharmaceutical research and the industry’s role in improving public health.
What is the difference between Phrma vs Medical Science Liaison?
| Aspect | Phrma | Medical Science Liaison |
|---|---|---|
| Required Credentials | Typically a PhD, PharmD, or MD | Usually a PhD, PharmD, or MD |
| Work Environment | Corporate, research, and development settings | Medical and scientific interactions with healthcare professionals |
| Employer & Industry Usage | Pharmaceutical companies, biotech firms | Pharmaceutical companies, medical affairs departments |
| Common Search & Comparison | Often compared for industry roles in pharma | Medical Science Liaison roles are frequently compared to Phrma positions |
While both Phrma and Medical Science Liaison roles require advanced degrees and are found within pharmaceutical companies, Phrma generally refers to the industry as a whole or to pharmaceutical companies, whereas Medical Science Liaisons are specific roles within those companies focused on scientific communication with healthcare professionals.
More about Phrma jobs
What job categories do people searching Phrma jobs look for? The top searched job categories for Phrma jobs are:
Other
Posted 26 days ago
Job description
Company Description
A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Required:
Business or Finance Bachelors or Associates Degrees
Working towards degree 3-5 Years of Pharmaceutical and/or Project Coordination experience.
Strong organization, financial and analytical skills.
Knowledge of accounting practices and procedures.
Knowledgeable about PhRMA, OIG and other industry regulations and guidelines as appropriate.
Primary Role Provide a brief summary
Summarize key areas of accountability and budget responsibility,
Manage day-to-day operations of 3rd party portal and registration site Provide ongoing assistance to site users
Review data entered by vendors to ensure accuracy.
Provide reports and metrics as requested. Provide feedback and recommendations as appropriate.
Provide feedback and recommendations as appropriate.
Seeks manager guidance, direction as needed Positive attitude, commitment to goals, demonstrates professionalism and operational leadership skills.
15%Consultancy Program Review Create and manage CPR calendar based on BU needs.
Coordinate and attend all meetings Prepare agenda and necessary materials and distribute to CPR Review Committee prior to meetings.
Provide on-going support as needed Responsible for Post meeting document collection. Understands OIG and other key regulatory guidelines.
Qualifications
Required:
Business or Finance Bachelors or Associates Degrees
Working towards degree 3-5 Years of Pharmaceutical and/or Project Coordination experience.
Strong organization, financial and analytical skills.
Knowledge of accounting practices and procedures.
Knowledgeable about PhRMA, OIG and other industry regulations and guidelines as appropriate.
Additional Information
Kind Regards
Sammeer Gaikwad
Operations Manager
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
(BOARD) # 732-549-2030 - Ext - 243
About Integrated Resources
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.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996