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Pharma Associate Jobs in Washington (NOW HIRING)

Pharma Expertise: Requires pharma and clinical trial processes and operations expertise; no ... Associate's with 12 years OR High school diploma / GED with 14 years of clinical execution ...

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Study Start-Up Associate II

Rockville, MD · Remote

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Master's Degree MS, MPH, PharmD (Preferred) * 1 to 3 years working within pharma and/or CRO ...

Data Science Associate

Chantilly, VA · On-site

$65K - $68K/yr

Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!With our sites in Chantilly and Manassas, Virginia ...

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Showing results 21-40

Pharma Associate information

What are the key skills and qualifications needed to thrive as a Pharma Associate?

To thrive as a Pharma Associate, you need a solid understanding of pharmaceutical products, regulatory compliance, and sales or customer service, often supported by a degree in pharmacy, life sciences, or a related field. Familiarity with CRM software, pharmaceutical databases, and knowledge of industry regulations such as FDA or EMA guidelines are typically required. Strong communication, relationship-building, and organizational skills help you effectively engage clients and manage multiple tasks. These skills are crucial for ensuring accurate information delivery, regulatory adherence, and successful client partnerships in a competitive industry.

What does a Pharma Associate do?

A Pharma Associate typically supports pharmaceutical operations, which may include working in research, development, quality assurance, regulatory affairs, or sales. Their responsibilities can involve assisting with clinical trials, ensuring compliance with regulations, preparing documentation, and collaborating with various teams to help bring pharmaceutical products to market. The specific duties of a Pharma Associate can vary depending on the department and company, but the role generally requires attention to detail and strong organizational skills. This position is often an entry-level step into the pharmaceutical industry, offering the opportunity to learn about drug development and regulatory processes.
What are the most commonly searched types of Pharma jobs in Washington? The most popular types of Pharma jobs in Washington are:
What are popular job titles related to Pharma Associate jobs in Washington? For Pharma Associate jobs in Washington, the most frequently searched job titles are:
Infographic showing various Pharma Associate job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Associate Director Study Start-up

Amgen SA

Washington, DC • On-site

$182.15 - $212.86/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New


Job description

Overview

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our mission is to serve patients living with serious illnesses.

Since 1980, we’ve helped pioneer biotech in our fight against the world’s toughest diseases. With focus on Oncology, Inflammation, General Medicine, and Rare Disease, we reach millions of patients each year. As a member of Amgen, you’ll help make a lasting impact on patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller lives.

Our culture is collaborative, innovative, and science-based. If you have a passion for challenges, you’ll thrive as part of the Amgen team. Join us and transform lives while transforming your career.

Study Start Up Hub – Associate Director Study Start-up What you will do

Let’s do this. Let’s change the world. In this vital role you will drive world-class study start-up planning and execution across a global portfolio, ensuring clinical trials launch with quality, efficiency, and speed.

  • Lead and manage a team of Study Start-up Managers, ensuring high-quality, compliant study start-up delivery across multiple programs and therapeutic areas.
  • Drive end-to-end study start-up planning and execution from global to local, delivering milestones on time, within budget, and in line with ICH-GCP and regulatory requirements.
  • Provide portfolio-level oversight of study start-up performance, resourcing, and delivery metrics, escalating risks with solution-focused recommendations.
  • Build team capability through coaching, mentoring, performance management, and role modelling of best practices in study start-up delivery.
  • Partner with functional and hub leaders to strengthen study start-up capabilities, ways of working, and operational readiness across the organisation.
  • Own and embed study start-up business processes, ensuring consistent application through training, knowledge sharing, and continuous improvement.
  • Foster a collaborative, high-engagement culture that encourages innovation, learning, and the sharing of knowledge and best practice.
  • Contribute to the evolution of the Study Start-up Hub model, shaping future ways of working through feedback, insights, and continuous improvement initiatives.
What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.

Basic Qualifications:
  • Pharma Expertise: Requires pharma and clinical trial processes and operations expertise; no relevant therapeutic knowledge required.
  • Management Experience: Requires experience leading and managing global teams and project management experience.
  • Tech Skills: No prior Veeva experience required.
  • Degree requirements: Doctorate with 3 years of clinical execution experience OR Master’s with 7 years OR Bachelor’s with 9 years OR Associate’s with 12 years OR High school diploma / GED with 14 years of clinical execution experience. In addition, at least 3 years of direct people management or leadership experience is required, which may run concurrently with the technical experience.
Preferred Qualifications:
  • 7 years of work experience in life sciences, focusing on clinical trials, including 5 years of biopharmaceutical clinical research experience obtained at a biotech or pharmaceutical company.
  • Experience managing multiple teams / direct reports across multiple clinical functions.
What you can expect of us

We support your professional and personal growth and well-being. From competitive benefits to a collaborative culture, we’ll support your journey every step of the way.

Compensation and Benefits

The annual base salary range for this opportunity in the U.S. is $182,145 - $212,860. In addition to base salary, Amgen offers a Total Rewards Plan including health and welfare plans, retirement savings, work-life balance, and career development opportunities, which may include:

  • Comprehensive benefits package including a Retirement and Savings Plan with company contributions, medical/dental/vision coverage, life and disability insurance, and flexible spending accounts.
  • Discretionary annual bonus program or sales-based incentive plan for field roles.
  • Stock-based long-term incentives.
  • Award-winning time-off plans and company-wide shutdowns.
  • Flexible work models, including remote work where possible.
Apply

Apply now for a career that defies imagination. Careers.amgen.com

Amgen is an Equal Opportunity employer. We will provide reasonable accommodations to applicants with disabilities where needed. Please contact us to request accommodation.

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