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Remote Pharmaceutical Research Jobs in Raleigh, NC

As a leading global contract research organization (CRO) with a passion for scientific rigor and ... Remote based in United States. What You'll Do * Coordinate and support delivery of Phase I clinical ...

We collaborate with top pharmaceutical and biotech companies to accelerate innovation and improve ... Flexible, remote work schedule. * Opportunity to contribute to global clinical research.

New

We collaborate with top pharmaceutical and biotech companies to accelerate innovation and improve ... Flexible, remote work schedule. * Opportunity to contribute to global clinical research.

New

Epidemiologist

Raleigh, NC · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Remote USA (EDT preferred) ICON is a global healthcare intelligence and clinical research ... preferably in a pharmaceutical or CRO setting * A strong desire to learn and gain a deep ...

Vice President, Medical Imaging

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Remote ICON is a global healthcare intelligence and clinical research organisation united by a ... both large pharmaceutical organizations and Contract Research Organizations (CROs), with ...

Sr Director, Nursing Services

Durham, NC · Remote

$116K - $324K/yr

In this remote role, you will work with some of the industry's most recognized pharmaceutical and ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...

Sr Director, Nursing Services

Durham, NC · Remote

$116K - $324K/yr

In this remote role, you will work with some of the industry's most recognized pharmaceutical and ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...

Showing results 41-60

Remote Pharmaceutical Research information

What is remote pharmaceutical research?

Remote pharmaceutical research refers to conducting various stages of drug discovery and development work from a location outside of a traditional laboratory or company office, often from home. This can include data analysis, literature reviews, clinical trial monitoring, regulatory documentation, and virtual collaboration with research teams. Advances in digital tools, secure data sharing, and teleconferencing have made it possible for many pharmaceutical research tasks to be performed remotely, increasing flexibility and access to a global talent pool.

How does collaboration typically work for professionals in remote pharmaceutical research roles?

In remote pharmaceutical research roles, collaboration is highly reliant on digital communication tools such as video conferencing, shared data platforms, and project management software. Researchers regularly participate in virtual meetings to discuss study progress, analyze data, and coordinate tasks with multidisciplinary teams, including scientists, regulatory specialists, and project managers. While working remotely can present challenges such as time zone differences and communication delays, most organizations have established structured workflows and regular check-ins to ensure alignment and maintain productivity. Strong written and verbal communication skills are essential for success in these roles.

What are the key skills and qualifications needed to thrive in remote pharmaceutical research, and why are they important?

To thrive in Remote Pharmaceutical Research, you need a solid background in life sciences or pharmacy, strong analytical skills, and experience with clinical research methodologies, often supported by an advanced degree. Familiarity with statistical analysis software, electronic data capture (EDC) systems, and regulatory compliance tools like Good Clinical Practice (GCP) certifications is crucial. Exceptional attention to detail, effective written communication, and self-motivation are valuable soft skills for remote collaboration and data interpretation. These skills ensure the integrity, accuracy, and regulatory compliance of research conducted outside traditional lab environments.

What are the most commonly searched types of Pharmaceutical Research jobs in Raleigh, NC?

The most popular types of Pharmaceutical Research jobs in Raleigh, NC are:

What are popular job titles related to Remote Pharmaceutical Research jobs in Raleigh, NC?

For Remote Pharmaceutical Research jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Pharmaceutical Research jobs in Raleigh, NC look for?

The top searched job categories for Remote Pharmaceutical Research jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Pharmaceutical Research jobs?

Cities near Raleigh, NC with the most Remote Pharmaceutical Research job openings:

Infographic showing various Remote Pharmaceutical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Full-time

Posted 13 days ago


Job description

About the Role

Medical Affairs at Azurity Pharmaceuticals, a privately held company delivering innovative medicines for overlooked patients across 50+ countries, drives scientific and clinical initiatives with a portfolio of 30+ brands spanning 10 dosage forms and 9 therapeutic areas. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

The Medical Manager CORE is a US-based position within the Medical Affairs Department, reporting to the VP Head of Medical - CORE. The role holder is responsible for leading and executing medical strategy to support the safe, effective, and evidence-based use of the company's products. This role serves as a scientific expert and key liaison between internal teams and external stakeholders, including healthcare professionals (HCPs), key opinion leaders (KOLs), and academic institutions.

Principle Responsibilities:

  • Develop and execute an integrated Medical Affairs strategy aligned with brand objectives and overall corporate priorities.
  • Serve as a scientific and clinical expert across the full product lifecycle, including prelaunch planning, launch execution, and postmarketing support.
  • Support and sustain strong relationships with key opinion leaders (KOLs) and other external scientific stakeholders.
  • Plan and support advisory boards, investigator meetings, and scientific symposia to advance scientific understanding and gather actionable insights.
  • Support the development, review, and approval of medical materials (e.g., slide decks, FAQs, training content) and support publication planning and execution (abstracts, posters, manuscripts) in close collaboration with Medical Excellence
  • Support stakeholder engagement and education planning in close collaboration with Medical Leads
  • Provide strategic medical input for conference planning, scientific content, and onsite execution.
  • Partner crossfunctionally with Clinical Development, Regulatory Affairs, Commercial, Market Access, and Pharmacovigilance to ensure aligned and effective execution of medical strategy.
  • Support sales and internal teams through medical training, scientific education, and ongoing clinical guidance.
  • Support realworld evidence (RWE), investigatorinitiated studies (IIS), and postmarketing studies in collaboration with Clinical Development as needed.
  • Collaborate with field medical team to analyze medical insights from external engagements to inform medical strategy and lifecycle planning.
  • Apply all Medical Affairs SOPs, regulatory, legal, and compliance guidelines while executing activities.
  • Demonstrate adaptability, focus, and composure in fast-paced settings while operating with minimal direction.

Qualifications and Education Requirements

Education:

  • Advanced terminal degree (PharmD, PhD, MD, DO,DNP) OR other advanced medical (NP, PA, RN etc.) is required.

Experience:

  • 2-3 years relevant work exp (clinical, fellowship, or research experience) and/or related pharmaceutical industry work experience is required.
  • Thorough knowledge or experience in cardiovascular, obesity, renal or endocrine related diseases.

Skills:

  • Excellent interpersonal and communication skills with a passion for excellence
  • Demonstrated ability to present effective and influential oral presentations
  • Deep scientific expertise - stays abreast of data, treatment trends, and new information in the profession and ability to articulate therapeutic knowledge and translate expert feedback into appropriate insights
  • Strong strategic and operational thinking skills, with the ability to manage effective networks
  • Ability to work effectively in a time and independently
  • Highly collaborative team player with experience working across cross-functional teams.
  • Excellent organization skills and decision-making abilities. Skillfully plans, prioritizes, and executes multiple responsibilities and projects.
  • Knowledge of relevant US healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends.
  • Proficiency in digital tools, AI
  • Travel: Up to 30-40% travel to attend medical conferences, engage with KOLs, and support strategic activities within the US.

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