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Prc Pharma Jobs (NOW HIRING)

VIVOS HOLDINGS

QA TECHNICIAN 1

Mooresville, IN

$19.50/hr

POSITION PURPOSE The Product Release Coordinator (PRC) is responsible for coordinating and ... Experience in an FDA regulated manufacturing environment (OTC, Pharma, Medical Device, Cosmetic, or ...

Thrive Global

Senior Manager, Healthcare Communications

$136K - $180K/yr

Working fluency in MLR/PRC review, FDA OPDP guidance, and the PhRMA Code (all defined below) Who You Are You've built your career at the intersection of pharma, communications, and complex program ...

Real Chemistry

Vice President, Omnichannel MarTech

$160K - $208K/yr

You bring hands-on experience delivering omnichannel platforms in pharma and understand how ... and MLR/PRC requirements from the start * Support commercial growth: Contribute to scoping ...

AstraZeneca

Associate Director, US Marketing, PNH

Boston, MA · On-site

$151K - $226K/yr

... PRC). What you will do: * Drive innovative and disruptive Marketing approaches aimed at expanding ... Advanced degree (MBA) * Pharma or biotech commercial experience, including hematology, oncology, or ...

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All JobsPrc Pharma Jobs

Prc Pharma information

See salary details

$20K

$47.5K

$105K

How much do prc pharma jobs pay per year?

As of Jul 15, 2026, the average yearly pay for prc pharma in the United States is $47,481.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,000.00 and $49,500.00 per year, depending on experience, location, and employer.

What are PRC Pharma professionals?

PRC Pharma professionals typically refer to individuals who work in pharmaceutical companies based in the People's Republic of China (PRC). These professionals may be involved in various aspects of the pharmaceutical industry, such as research and development, regulatory affairs, sales, marketing, and manufacturing of pharmaceutical products. Their roles often require knowledge of both domestic and international pharmaceutical regulations, drug development processes, and the unique aspects of the Chinese healthcare market. PRC Pharma professionals play a vital role in ensuring that medicines are safely developed, produced, and delivered to patients in China and around the world.

What are the key skills and qualifications needed to thrive as a PRC Pharmacist, and why are they important?

To thrive as a PRC Pharmacist, you need a solid foundation in pharmacy practice, drug dispensing, and clinical pharmacology, typically backed by a Bachelor of Science in Pharmacy and a valid PRC license. Familiarity with pharmacy management systems, automated dispensing tools, and regulatory compliance protocols is essential. Strong attention to detail, customer service skills, and the ability to communicate complex information clearly are crucial soft skills in this role. These competencies ensure safe medication practices, legal compliance, and effective patient care in both retail and hospital pharmacy settings.

What are some common challenges faced by professionals in PRC Pharma roles, and how can they be addressed?

Professionals in PRC (Pharma Regulatory Compliance) roles often navigate the complex and evolving landscape of pharmaceutical regulations and standards. Keeping up with frequent regulatory updates, ensuring timely submission of accurate documentation, and coordinating with cross-functional teams can be challenging. Building strong organizational skills, maintaining open lines of communication with colleagues in R&D, quality assurance, and legal departments, and participating in ongoing training can help address these challenges effectively. Staying proactive and detail-oriented is essential for success in this dynamic environment.

What is the difference between Prc Pharma vs Pharmaceutical Sales Representative?

AspectPrc PharmaPharmaceutical Sales Representative
Required CredentialsDegree in pharmacy, life sciences, or related field; certifications may be preferredDegree in life sciences, marketing, or related field; often requires pharmaceutical industry knowledge
Work EnvironmentLaboratory, manufacturing facilities, or quality control settingsField-based, visiting healthcare providers and pharmacies
Employer & Industry UsagePharmaceutical manufacturing companies, biotech firmsPharmaceutical companies, medical device firms
Common Search & Comparison IntentUnderstanding roles in pharma manufacturing and quality controlSales strategies, product knowledge, and industry roles

While Prc Pharma typically refers to professionals involved in pharmaceutical manufacturing, quality control, or regulatory roles, Pharmaceutical Sales Representatives focus on promoting and selling pharmaceutical products to healthcare providers. Both roles require industry knowledge but differ in daily tasks and work environments.

More about Prc Pharma jobs
What job categories do people searching Prc Pharma jobs look for? The top searched job categories for Prc Pharma jobs are:
Prc Pharma jobs near you
Infographic showing various Prc Pharma job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 93% Full Time, 2% Part Time, 1% Temporary, and 3% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $47,481 per year, or $22.8 per hour.
PRC (Promotional Review Committee) Coordinator

PRC (Promotional Review Committee) Coordinator

Inficare Technologies

Remote

Full-time

Posted 9 days ago

Job description

PRC (Promotional Review Committee) Coordinator - Onshore/Nearshore
Industry: Life Sciences / Pharma / Biotech
Work Model: Onshore (US) or Nearshore (LATAM / Canada support for US teams)
Role Overview
The PRC Coordinator manages the end-to-end promotional review process for marketing and medical materials, ensuring compliance with regulatory, legal, and brand standards. This role serves as the operational backbone of the PRC process, coordinating cross-functional stakeholders (Marketing, Medical, Legal, Regulatory) and optimizing review cycles.
Key Responsibilities
  • Coordinate and facilitate PRC review cycles for promotional and non-promotional materials (digital, print, HCP/patient-facing)
  • Manage submissions through systems such as Veeva PromoMats / Vault, Aprimo, or similar platforms
  • Schedule and lead PRC meetings, ensuring stakeholder alignment and timely reviews
  • Track material status, comments, approvals, and version control
  • Consolidate and reconcile cross-functional feedback into actionable updates for stakeholders
  • Ensure adherence to MLR compliance, FDA/OPDP guidelines, and internal SOPs
  • Maintain and report on KPIs (cycle time, approval timelines, review efficiency)
  • Identify process improvement opportunities for review cycle optimization
  • Support audits by maintaining accurate documentation and audit trails
  • Act as liaison between marketing teams and reviewers, ensuring clarity and efficiency

Required Qualifications
  • Bachelor's degree (Life Sciences, Business, Marketing, or related field)
  • 3-8 years of experience in:
    • PRC / MLR coordination
    • Marketing operations or regulatory support in pharma/biotech
  • Hands-on experience with Veeva Vault PromoMats (preferred) or similar tools
  • Strong understanding of promotional compliance and review workflows
  • Excellent organizational and project management skills
  • Ability to manage multiple deadlines in fast-paced environments
  • Strong communication and stakeholder management skills

Preferred Skills
  • Familiarity with US pharma regulatory environment (FDA, OPDP)
  • Experience supporting commercial launch or brand teams
  • Exposure to digital asset review and omnichannel campaigns
  • Data tracking/reporting via Excel, Power BI, or dashboards
  • Lean/Six Sigma or process improvement mindset

Onshore vs. Nearshore Expectations
Onshore (US-based):
  • Direct engagement with brand, medical, legal teams
  • Participation in live PRC discussions and decision-making forums
  • Greater ownership of stakeholder management and escalation handling

Nearshore (LATAM/Canada):
  • Operational execution of review coordination, tracking, and documentation
  • Time-zone aligned support for US teams
  • Increasing exposure to stakeholder interaction depending on seniority

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