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Rtp Pharma Jobs (NOW HIRING)

Biogen

NC · On-site

$160K - $220K/yr

... in RTP, NC, ensuring they are delivered on time, within budget, and with minimal oversight. Your ... Pharma-Biotech industry. * Significant program leadership experience in Patient Services and/or ...

Kymanox

$180 - $320/hr

... big pharma organizations. Kymanox's engineering, scientific, and CGxP compliance professionals ... Kymanox is headquartered in Research Triangle Park (RTP), North Carolina, USA and operates ...

Fujifilm

QC LIMS Developer

Durham, NC · On-site

... RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top ... Master's a plus. * 3-7 years configuring and supporting LIMS in GMP environments (pharma/biotech ...

Fujifilm

QC LIMS Developer

Research Triangle Park, NC · On-site

... RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top ... Master's a plus. * 3-7 years configuring and supporting LIMS in GMP environments (pharma/biotech ...

AskBio Inc.

$90 - $130/hr

This position is on site in RTP, NC and reports to an Associate Director, Clinical Immunology. Job ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...

Zifo

LIMS Analyst (LabVantage)

Boston, MA

San Francisco Bay Area, Tri-state Area (NY, NJ, PA), RTP (NC) We are seeking a Laboratory ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

Fujifilm

QC LIMS Developer

Research Triangle Park, NC · On-site

... RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top ... Master's a plus. * 3-7 years configuring and supporting LIMS in GMP environments (pharma/biotech ...

AskBio

Associate Scientist, Immunology

Durham, NC · On-site

This position is on site in RTP, NC and reports to an Associate Director, Clinical Immunology. Job ... Prior experience in Pharma or CRO industry * Basic lab skills, such as adhering GCLP, biosafety and ...

Kymanox

Senior Vice President, Commercial

Morrisville, NC · On-site

$180 - $320/hr

... big pharma organizations. Kymanox's engineering, scientific, and CGxP compliance professionals ... Kymanox is headquartered in Research Triangle Park (RTP), North Carolina, USA and operates ...

Zifo

LIMS Analyst (LabVantage)

Boston, MA · On-site

San Francisco Bay Area, Tri-state Area (NY, NJ, PA), RTP (NC) We are seeking a Laboratory ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

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How much do rtp pharma jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for rtp pharma in the United States is $26.57, according to ZipRecruiter salary data. Most workers in this role earn between $15.87 and $36.30 per hour, depending on experience, location, and employer.

What is an RTP Pharma?

An RTP Pharma job typically refers to a role in the pharmaceutical industry located in Research Triangle Park (RTP), North Carolina. RTP is a major hub for biotech and pharmaceutical companies, offering positions in research, development, manufacturing, and regulatory affairs. Job responsibilities vary but often include drug formulation, clinical trials, quality control, and compliance with industry regulations. Positions may be available for scientists, engineers, technicians, and regulatory specialists.

What are the main responsibilities and typical work environment for an RTP Pharma professional?

RTP Pharma professionals are commonly involved in research, testing, and formulation of pharmaceutical products, ensuring compliance with regulatory standards and company protocols. The work environment often includes both laboratory settings and office-based tasks, with frequent collaboration across multidisciplinary teams such as research, quality assurance, and regulatory affairs. Daily responsibilities may include conducting experiments, analyzing data, preparing documentation, and participating in meetings to discuss project progress. Collaboration and adaptability are key, as projects are often driven by strict deadlines and evolving scientific challenges.

What are the key skills and qualifications needed to thrive in the RTP Pharma position, and why are they important?

To thrive as an RTP Pharma professional, you generally need a strong background in pharmaceutical sciences, regulatory compliance, and drug development processes, often supported by a relevant bachelor's or advanced degree. Familiarity with laboratory information management systems (LIMS), quality assurance protocols, and industry-specific certifications such as Good Manufacturing Practices (GMP) is highly valuable. Strong analytical thinking, attention to detail, and effective communication skills help professionals collaborate effectively and ensure accurate documentation. These skills are vital to maintaining regulatory standards, advancing product development, and ensuring the safety and efficacy of pharmaceuticals.

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Rtp Pharma jobs near you
Infographic showing various Rtp Pharma job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 90% Full Time, 2% Part Time, 5% Contract, and 1% Nights. Highlights an 82% Physical, 4% Hybrid, and 14% Remote job distribution, with an average salary of $55,272 per year, or $26.6 per hour.

Associate Director, Program Management, Global Commercial Medical IT

Biogen

NC • On-site

$160K - $220K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Key responsibilities

  • Lead highly complex cross-functional projects and programs, including Patient Services initiatives, product launch programs, and mergers & acquisitions.

  • Consolidate project and program-level status reporting into a comprehensive portfolio view and support month-end and portfolio reporting focusing on financials and performance metrics.

  • Identify and resolve issues to keep projects on track, and proactively manage stakeholder expectations and deliverables.

Biogen rating

9.3

Company rating: 9.3 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

3rd of 86 rated pharmaceutical

Job description

About This Role:
As the Associate Director of Program Management within the Global Commercial and Medical (GCM) IT organization, you will lead intricate, cross-functional programs and oversee portfolio financials, including governance, annual budgeting, and month-end close. You will drive critical projects and product launches supporting our Patient Services Organization in RTP, NC, ensuring they are delivered on time, within budget, and with minimal oversight. Your role is pivotal in collaborating with stakeholders to drive decisions and proactively manage and mitigate issues and risks, consolidate portfolio-level status reporting and track performance, ensuring the portfolio delivers high-quality outcomes. You will support the GCM Leadership Team with monthly portfolio reviews and manage ad hoc requests as needed. Reporting to the Director of Portfolio Management and Operations for Global Commercial and Medical IT, you will be a key player in driving the success and efficiency of our organizational projects.
What You'll Do:
  • Lead highly complex cross-functional projects and programs, including Patient Services initiatives, product launch programs and mergers & acquisitions.
  • Consolidate project and program-level status reporting into a comprehensive portfolio view.
  • Support month-end and portfolio reporting, focusing on financials and performance metrics.
  • Drive large programs to ensure alignment on scope, schedule, resources, and budgets.
  • Proactively manage key stakeholders, ensuring accountability and timely completion of deliverables.
  • Clearly communicate financial status, schedule, risks, and changes to all stakeholders.
  • Facilitate cross-team discussions for integrated project plans and communications.
  • Identify and resolve issues to keep projects on track.
  • Review financials for the GCM IT portfolio, ensuring accuracy and adherence to financial calendars.
  • Identify efficiencies and areas of improvement for portfolio operations.

Who You Are:
You are a strategic thinker who thrives in managing complex and cross-functional programs. Your attention to detail and organizational skills ensure that projects are delivered with precision and high quality. You possess excellent communication skills that keep stakeholders informed and engaged, and you excel at managing financials and identifying areas for improvement. You work well under pressure, maintaining focus and delivering results with minimal supervision. Your ability to manage shifting priorities and timelines makes you an invaluable asset to our team.
Required Skills:
  • A Master's degree in Information Technology, an MBA preferred or equivalent experience.
  • 10+ years of experience as an IT professional managing projects, programs, and portfolios in the Pharma-Biotech industry.
  • Significant program leadership experience in Patient Services and/or Patient Support Organizations.
  • 5+ years of experience implementing complex, cross-functional projects within established software development life cycle methodologies.
  • Experience managing projects through waterfall, agile, or SAFe delivery methodologies.
  • Strong organizational skills and attention to detail.
  • Financial discipline and accountability for deliverables.
  • Excellent verbal and written communication skills.
  • Ability to manage shifting priorities and timelines effectively.

Preferred Skills:
  • Experience managing product launches and/or mergers & acquisitions.
  • Process-oriented mindset with the ability to identify efficiencies.

Job Level: Management
Additional Information
The base compensation range for this role is: $160,000.00-$220,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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About Biogen

Sourced by ZipRecruiter

At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.

Industry

Scientific research and development services

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

1978

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