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Clinical Data Associate Remote Jobs in Delaware (NOW HIRING)

Clinical Affairs Scientist

Wilmington, DE ยท On-site +1

$105K - $197K/yr

... Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and ... Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms.

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 ...

Coding Coordinator IV - (Remote)

Newark, DE ยท On-site +1

$32.77 - $52.43/hr

Analyze clinical data of inpatients, current treatment, past medical history and identifies potential gaps in physician documentation. * Analyze and report trends for improvement opportunities in ...

Collaborate with Dutch's clinical leadership team as needed What Makes This Role Unique * Flexible ... If you would like more information about how your data is processed, please contact us. apply for ...

Collaborate with Dutch's clinical leadership team as needed What Makes This Role Unique * Flexible ... If you would like more information about how your data is processed, please contact us. apply for ...

Litigation Associate - Complex Commercial Matters Wilmington, DE (Hybrid or Remote Flexibility ... Cyber/Data Security * Employment Law * Premises Liability * Professional Liability * Construction

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Clinical Data Associate Remote information

What is a clinical data associate?

A Clinical Data Associate (Remote) is a professional who manages and verifies data collected during clinical trials, working from a remote location. They ensure the accuracy, integrity, and confidentiality of clinical trial data, collaborating with clinical teams and using specialized software. Their responsibilities include data entry, cleaning, validation, and generating reports to support regulatory submissions. Remote Clinical Data Associates utilize secure systems to access and manage data, allowing them to efficiently support clinical research from anywhere.

What are the key skills and qualifications needed to thrive as a clinical data associate?

To thrive as a Clinical Data Associate (Remote), you need a strong background in life sciences, data management, and an understanding of clinical trial processes, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical data management software, and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, problem-solving abilities, and effective virtual communication are crucial soft skills for managing data integrity and collaborating with remote teams. These skills and qualifications ensure the accurate collection, validation, and reporting of clinical trial data, which is essential for regulatory compliance and successful study outcomes.

What are some common challenges faced by a clinical data associate working remotely, and how can they be managed?

Clinical Data Associates working remotely often face challenges related to communication and maintaining data quality standards across distributed teams. It can be more difficult to collaborate with clinical research coordinators, data managers, and other stakeholders without in-person interactions, making clear and timely communication essential. Utilizing secure data management platforms, participating in regular virtual meetings, and adhering strictly to data integrity protocols can help address these challenges. Proactively seeking feedback and staying updated on regulatory changes also contribute to maintaining high standards while working remotely.

What is the difference between Clinical Data Associate Remote vs Clinical Data Coordinator?

AspectClinical Data Associate RemoteClinical Data Coordinator
CredentialsBachelor's in life sciences or related field; familiarity with data management systemsBachelor's in health sciences or related field; experience with clinical data
Work EnvironmentRemote, primarily computer-basedTypically on-site or hybrid, working with clinical teams
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites
Search & Comparison IntentYesYes

The Clinical Data Associate Remote and Clinical Data Coordinator roles share similarities in required education and industry usage. However, Clinical Data Associate Remote positions are primarily remote and focus on data entry and management from a distance, while Clinical Data Coordinators often work on-site, coordinating data collection and quality at clinical sites. Both roles are essential in clinical research but differ mainly in work setting and specific responsibilities.

What are popular job titles related to Clinical Data Associate Remote jobs in Delaware?

For Clinical Data Associate Remote jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Clinical Data Associate Remote jobs in Delaware look for?

The top searched job categories for Clinical Data Associate Remote jobs in Delaware are:

What cities in Delaware are hiring for Clinical Data Associate Remote jobs?

Cities in Delaware with the most Clinical Data Associate Remote job openings:

Infographic showing various Clinical Data Associate Remote job openings in Delaware as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% Remote job distribution.

Associate Director Radiopharmaceutical Clinical Applications - Mid-Atlantic (NJ, PA, Washington D...

Bethany Beach, DE โ€ข Remote

Lantheus
Pharmaceutical and Medicine Manufacturingย โ€ขย 501 - 1,000 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago


Job description

Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and United Kingdom, Lantheus has been providing radiopharmaceutical solutions for nearly 70 years.

Today, weโ€™re expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world.

At Lantheus we are purpose-driven, and every employee plays a vital role in our success. Weโ€™re dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress.

Join us and be part of a company where your contributions make a real impact, because we know someoneโ€™s health is in our hands.

Summary of role

The Radiopharmaceutical Clinical Applications Associate Director will be responsible for leading the clinical application efforts regionally for our radiopharmaceutical products. This role involves building and maintaining relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs), providing advanced clinical and technical expertise, and ensuring the optimal use of our products in the clinical setting. The position will also support field research initiatives, provide educational training, and ensure compliance with industry regulations and company policies.

This is a remote position open to applicants authorized to work for any employer within the United States. The territory includes NJ, PA, Washington DC, MD, DE.

Responsibilities

  • Identify, develop, and engage in long-term relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs) in the assigned territory, including Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Safety Officers, Health Physicists, Nursing Staff, and Advanced Practice HCPs at imaging facilities and medical centers.
  • Provide training to imaging/treatment centers on handling, administration, and radiation safety of current products, including initial and re-training sessions.
  • Educate on-site preparation and infusion processes for products, including radiopharmaceutical licensing, supporting approved imaging/therapies, and clinical trials.
  • Educate the HCP community to ensure they have the proper knowledge and technical expertise to use Lantheus products safely and effectively.
  • Utilize clinical and technical expertise to institutional workflows, regional diagnostic imaging patterns, treatment guidelines, and therapeutic advances in oncology and molecular imaging. Gather insights into the needs and interests of healthcare providers and the medical needs of patients with a focus on Lantheus approved and investigational agents.
  • Maintain thorough and up-to-date knowledge of imaging techniques, clinical information, and product data in the diagnostic and therapeutic radiopharmaceutical field.
  • Respond appropriately and document accurate scientific data in response to unsolicited questions from customers about approved and investigational products.
  • Support Lantheus Field Research Initiatives, including Investigator Sponsored Trials (ISTs), the Image Library, and Clinical Trials aligned with the Lantheus pipeline.
  • Attend national congresses and meetings, providing medical and scientific booth support as requested, in compliance with industry regulations.
  • Fully understand and comply with all Lantheus SOPs, working procedures, and corporate requirements.
  • Adhere to the US โ€œCompliance Code of Conductโ€ and all LMI policies and procedures, the OIG Guidance, the PhRMA Code, GCP, HIPPA and relevant FDA laws and regulations (certify completion where required).

Basic Qualifications

  • Minimum Bachelorโ€™s Degree Required
  • 4+ years Nuclear Medicine Technologist, Clinical Application Specialist, or similar/relevant experience.
  • 2+ years Clinical experience in oncology, urology, neurology or radiopharmaceuticals/medical imaging
  • Exceptional communicator and presenter with proven oral and written communications skills.
  • Advanced understanding of current and emerging trends in the field of Nuclear Medicine, radiopharmaceuticals, and diagnostic imaging.
  • Proficient at translating and communicating approved scientific or clinical data into high quality medical information appropriate to the audiences engaged.
  • Demonstrated success working in a team environment, communicating clearly and effectively with management, peers, and all cross-functional teams.
  • Highly motivated to achieve optimal results with a demonstrated record of career growth and achievement.
  • Proven ability to successfully manage multiple tasks simultaneously and adapt to and communicate change.

Other Requirements

  • Advanced Word, PowerPoint, and Excel skills
  • 60% Travel required; reside near an international airport

The pay range for this position is between $163,000 and $245,000 annually.

Actual base pay offered may vary depending on a number of factors such as job-related knowledge, skills and experience. Employees in this position are eligible for a discretionary performance-based cash incentive. Benefits for this position include a comprehensive health benefits package that includes medical, prescription drug, dental, and vision coverage. Other offerings include life and disability benefits, pre-tax accounts, a 401(k) with company contribution, and a variety of other benefits. In addition, employees are eligible for a generous time off package including paid vacation, holidays, sick days, and paid parental leave. Interested candidates can apply at Lantheus.com. Applications for this position will be accepted until July 30, 2026.

Lantheus is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression, sexual orientation, marital status, military service and veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any characteristic protected under applicable federal, state, or local laws and ordinances.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition teamย at talentacquisition@lantheus.com.

Lantheus is an E-Verify Employer.

Applicants have rights under Federal Employment Law:ย Employee Polygraph Protection Act (EPPA);ย Family and Medical Leave Act (FMLA)
For California Applicants:ย Family Care & Medical Leave & Pregnancy Disability Leave;ย California Law Prohibits Workplace Discrimination & Harassment;ย Your Rights and Obligations as a Pregnancy Employee
For Ohio Applicants:ย Know Your Rights: Equal Employment Opportunity is the Law