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Clinical Research Biotech Remote Jobs in Delaware

AstraZeneca

Clinical Research Associate

Wilmington, DE · On-site +1

As a Clinical Research Associate, you will be the face of AstraZeneca at investigative sites ... Plan and conduct remote and onsite monitoring visits per the Monitoring Plan; perform source data ...

Amgen

Imaging Specialist Manager

Wilmington, DE · On-site +1

Experience in life sciences or medical fields, including imaging expertise and clinical research acquired working on clinical trials at a biotech, pharmaceutical or CRO company, having a strong ...

Roquette

BioPharma Business Developer

Wilmington, DE · On-site +1

$132K - $198K/yr

... remote depending on business needs. Compensation: The current salary range for this role is ... Bachelor's or University Degree in Pharmacy, Chemistry, Life Sciences, Biotechnology, Chemical ...

Moderna

$20 - $60/hr

... clinical trials and commercial licensure. You will apply your educational background and learn new ... remote work . Here's What You'll Do * Work with a team of highly skilled experts to come up to ...

Moderna

$20 - $60/hr

... clinical trials and commercial licensure. You will apply your educational background and learn new ... remote work . Here's What You'll Do * Work with a team of highly skilled experts to come up to ...

Moderna

$20 - $60/hr

... clinical trials and commercial licensure. You will apply your educational background and learn new ... remote work . Here's What You'll Do * Work with a team of highly skilled experts to come up to ...

Moderna

Intern, CMC Development (Summer 2027)

Milford, DE · On-site +1

$20 - $60/hr

... clinical trials and commercial licensure. You will apply your educational background and learn new ... remote work . Here's What You'll Do * Work with a team of highly skilled experts to come up to ...

Moderna

Intern, CMC Development (Summer 2027)

Smyrna, DE · On-site +1

$20 - $60/hr

... clinical trials and commercial licensure. You will apply your educational background and learn new ... remote work . Here's What You'll Do * Work with a team of highly skilled experts to come up to ...

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Clinical Research Biotech Remote information

What does a clinical research biotech remote professional do?

A Clinical Research Biotech Remote professional manages and oversees clinical trials and research studies for biotech companies while working from a remote location. Their responsibilities typically include coordinating study protocols, ensuring regulatory compliance, collecting and analyzing data, and collaborating with investigators and other stakeholders virtually. By working remotely, these professionals use digital tools to monitor trial progress and maintain communication with research teams, sponsors, and regulatory bodies. Their work plays a crucial role in advancing new biotech therapies and medical technologies.

How does a clinical research biotech remote professional collaborate with cross-functional teams?

In a remote Clinical Research Biotech role, professionals frequently collaborate with cross-functional teams, including clinical operations, regulatory affairs, data management, and biostatistics. Communication typically occurs via video conferences, collaborative platforms, and shared digital workspaces. Successful candidates should be comfortable navigating time zone differences and proactively sharing updates to ensure project milestones are met. Building strong virtual relationships and maintaining transparency are key to overcoming challenges and ensuring seamless trial execution.

What are the key skills and qualifications needed to thrive as a clinical research biotech remote professional?

To thrive as a Clinical Research Biotech professional working remotely, you typically need a background in life sciences, experience in clinical research methodologies, and familiarity with regulatory requirements such as GCP and FDA guidelines. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and remote collaboration tools is essential. Strong organizational skills, self-motivation, and effective virtual communication set top performers apart in remote environments. These abilities are crucial for ensuring regulatory compliance, maintaining data integrity, and collaborating efficiently across dispersed teams.

What is the difference between Clinical Research Biotech Remote vs Clinical Research Associate?

AspectClinical Research Biotech RemoteClinical Research Associate
CredentialsBachelor's degree in life sciences; certifications like CCRP or RACBachelor's degree in life sciences; often required certifications like CCRP
Work EnvironmentRemote, flexible locationTypically on-site or travel-based, but remote options are increasing
Employer & IndustryBiotech companies, pharmaceutical firms, CROsPharmaceutical companies, CROs, biotech firms
Job FocusSupporting clinical trials remotely, data management, regulatory complianceMonitoring clinical trials, site visits, ensuring protocol adherence

While both roles involve clinical trial support, Clinical Research Biotech Remote focuses on remote data and regulatory tasks within biotech companies, whereas Clinical Research Associate typically involves on-site monitoring and site management. The remote role offers flexibility, while the CRA role emphasizes direct site interaction.

What are popular job titles related to Clinical Research Biotech Remote jobs in Delaware?

For Clinical Research Biotech Remote jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Clinical Research Biotech Remote jobs in Delaware look for?

The top searched job categories for Clinical Research Biotech Remote jobs in Delaware are:

What cities in Delaware are hiring for Clinical Research Biotech Remote jobs?

Cities in Delaware with the most Clinical Research Biotech Remote job openings:

Clinical Research Biotech Remote jobs near you
Infographic showing various Clinical Research Biotech Remote job openings in Delaware as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Clinical Research Associate

Wilmington, DE • On-site, Remote

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees
Learn more about AstraZenecaexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical

Job description

Are you ready to turn rigorous site execution into faster access to life-changing medicines for patients? As a Clinical Research Associate, you will be the face of AstraZeneca at investigative sites, ensuring our studies are initiated, conducted, and closed with excellence so regulators can make decisions with confidence.
In this role, you will drive the quality, speed, and integrity of clinical delivery across assigned sites. You will combine risk-based insight with hands-on partnership, building trusted relationships with investigators and site staff while keeping participant safety and data robustness at the forefront. Do you thrive on solving problems in real time and translating complex protocols into confident, compliant site performance?
From day one, you will contribute to a nimble, outcome-focused team that values curiosity, accountability, and collaboration. Your impact will be tangible-measured in inspection-ready sites, reliable data, strong recruitment, and study milestones achieved on schedule.
Accountabilities:
  • Site Readiness and Initiation: Qualify and select investigators; manage start-up activities as required, including document preparation, ethics/regulatory submissions, and site initiation. Ensure site teams complete all required training and remain inspection-ready throughout the study.
  • Risk-Based Monitoring: Plan and conduct remote and onsite monitoring visits per the Monitoring Plan; perform source data verification/review; complete remote data checks; use Site Quality Risk Assessments to adjust monitoring intensity and focus on what matters most.
  • Data Quality and Systems Excellence: Maintain up-to-date, accurate entries in CTMS and other systems; collaborate with data management to resolve queries promptly; prepare clear, timely monitoring reports and follow-up letters; collect and quality-check essential documents in the eTMF.
  • Patient Safety Oversight: Ensure accurate and prompt reporting of Serious Adverse Events and follow-up; verify protocol adherence; safeguard participant rights, privacy, and wellbeing at every step.
  • Site Performance and Recruitment: Track and drive enrollment and retention; proactively identify risks and issues; implement corrective and preventive actions; escalate appropriately; follow through to resolution to protect timelines and quality.
  • Investigational Product and Materials: Manage study supplies and the Investigator Site File; oversee investigational product accountability and preparation for destruction, where applicable.
  • Compliance and Inspection Readiness: Adhere to ICH-GCP, local regulations, and AstraZeneca procedures; escalate quality or compliance concerns; prepare sites and collaborate during audits and regulatory inspections.
  • Stakeholder Collaboration: Engage actively with the Local Study Team and investigators; contribute to investigator meetings; communicate progress and insights; share site intelligence that informs strategy; collaborate with cross-functional colleagues as directed.
  • Continuous Improvement: Identify and champion more efficient, cost- and time-optimized delivery of quality clinical trials; apply risk-based thinking to streamline processes and improve outcomes over the course of the study.

Essential Skills/Experience:
  • Bachelor's degree in related discipline, preferably in life science, and ensures successful conduct of responsibilities and appropriate interactions with internal and or external stakeholders.
  • Relevant knowledge and ability to fulfil key responsibilities, including but not limited to: Drug development process, international guidelines ICH-GCP, relevant country regulations, medical knowledge and ability to learn relevant AZ Therapeutic Areas, Clinical Study Management including monitoring, study drug handling and data management.

Role Required Skills
  • Personal Effectiveness & Drives Self-Accountability
  • Learning Agility
  • Financial, Technology & Process Competency
  • Active Listening, Fluency in written & spoken business-level English
  • Act with Integrity & high ethical standards
  • Effectively work as part of a team, in person and virtual settings, demonstrates cultural awareness
  • Identify and champion more efficient delivery of quality clinical trials with optimised cost and time.
  • Ability to travel nationally/internationally as required.
  • Valid driving license, if country employment requirement
  • Communication & Teamwork - Impactful Site conversations
  • Effective, risk-based thinking - Plans & Aligns, Strategic thinking, Problem Solving, Critical Thinking, Decision Making, Effective Issue Management
  • Ethical & Participant Safety Considerations - Interpret and Implement the Clinical Study Protocol; Adhere to Participant Rights, Privacy and Wellbeing; Participant Safety Oversight and Reporting
  • Clinical Study Operations (GCP) & Quality Management - Audit & Inspection Readiness, RbQM: Interpreting and implementing the Monitoring Plan; Source Documentation and Effective Source Data Verification/Review (SDV/SDR)
  • Deliver Priorities Results & Impact: Recruitment/Retention Planning & Action.

Desirable Skills/Experience:
  • Prior experience delivering multi-center clinical studies as a CRA across phases.
  • Hands-on experience with CTMS, eTMF, and risk-based monitoring, including remote monitoring approaches.
  • Experience in start-up activities and submissions to Ethics Committees/IRBs and Regulatory Authorities.
  • Exposure to audits and inspections with proven inspection-readiness practices.
  • Certification such as ACRP-CCRA or SOCRA.
  • Strong command of local language(s) in addition to English.
  • Experience across multiple therapeutic areas and complex protocols.
  • Comfort with data analytics or digital tools used in clinical operations.

Why AstraZeneca:
Join a science-led organization where your fieldwork directly accelerates decisions that bring new medicines to people who need them. You will collaborate closely with colleagues across development, often bringing diverse experts together to challenge ideas and move faster with balanced risk. We value curiosity alongside accountability and kindness; leaders remove barriers so you can focus on what matters-patient safety, data quality, and timely delivery. With modern tools, a culture that welcomes bold thinking, and opportunities to grow across varied projects, your contributions will shape both our pipeline and your career.
Seize this opportunity to elevate your impact-help deliver confident, fast approvals by turning exceptional site execution into better outcomes for patients and your own growth.
The annual base pay (or hourly rate of compensation) for this position ranges from $112,154.40 - $168,231.60 USD Annual, either as annual base pay or as the hourly rate (annual base pay divided by 2080 hours)]. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
27-Aug-2026
Closing Date
12-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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