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Clinical Research Pre Screening Jobs in Delaware

Christiana Care

Hematologist - Newark, DE

Newark, DE · On-site

QOPI certified, strong clinical research, NCORP Alliance, and NRG Pharmaceutical trials. * Located ... screening and referrals based on your personal and family medical history. * We are the only ...

Direct Jobs

Experienced Medical Oncologist

Newark, DE · On-site

$387.36 - $639.03/hr

QOPI certified, strong clinical research, NCORP Alliance, and NRG Pharmaceutical trials. * Located ... screening and referrals based on your personal and family medical history. * We are the only ...

Direct Jobs

Hematologist - Newark, DE

Newark, DE · On-site

$387.36 - $639.03/hr

QOPI certified, strong clinical research, NCORP Alliance, and NRG Pharmaceutical trials. * Located ... screening and referrals based on your personal and family medical history. * We are the only ...

ChristianaCare

Hematologist - Newark, DE

Newark, DE · On-site

QOPI certified, strong clinical research, NCORP Alliance, and NRG Pharmaceutical trials. * Located ... screening and referrals based on your personal and family medical history. * We are the only ...

Christiana Care

Experienced Medical Oncologist

Newark, DE · On-site

$196.25/hr

QOPI certified, strong clinical research, NCORP Alliance, and NRG Pharmaceutical trials. * Located ... screening and referrals based on your personal and family medical history. * We are the only ...

ChristianaCare

Experienced Medical Oncologist

Newark, DE · On-site

$195.50/hr

QOPI certified, strong clinical research, NCORP Alliance, and NRG Pharmaceutical trials. * Located ... screening and referrals based on your personal and family medical history. * We are the only ...

The IMA Group

Medical Assistant- Dover, DE

Dover, DE

$18.50/hr

Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public ... Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple ...

The IMA Group

Medical Assistant- Dover, DE

Dover, DE · On-site

$18.50/hr

Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public ... Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple ...

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All JobsClinical Research Pre Screening JobsClinical Research Pre Screening Jobs in Delaware

Clinical Research Pre Screening information

What is a clinical research pre screening specialist?

A Clinical Research Pre Screening specialist is responsible for evaluating potential participants to determine if they meet the basic eligibility criteria for clinical trials. They typically review medical histories, conduct initial assessments, and communicate with patients about the study requirements. This role is crucial in ensuring that only suitable candidates proceed to the next stages of the clinical trial process, which helps maintain the integrity and safety of the research. Pre screening specialists often work closely with clinical research coordinators and investigators.

What are the key skills and qualifications needed to thrive as a clinical research pre screening specialist?

To thrive as a Clinical Research Pre-Screening Specialist, you need a background in life sciences or healthcare, knowledge of research protocols, and attention to regulatory guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Strong interpersonal skills, attention to detail, and effective communication help in accurately evaluating candidates and collaborating with research teams. These skills ensure the accurate identification of eligible participants, compliance with study requirements, and smooth progression of clinical trials.

What is the difference between Clinical Research Pre Screening vs Clinical Research Coordinator?

AspectClinical Research Pre ScreeningClinical Research Coordinator
Primary RoleInitial participant eligibility assessment and screeningOversees entire study process, including recruitment, data collection, and follow-up
Required CredentialsHigh school diploma or equivalent; some roles may require clinical or research certificationsBachelor's degree in health or related field; often requires clinical research certification
Work EnvironmentScreening sites, clinics, or research facilitiesResearch sites, hospitals, clinics, or research institutions
Employer & Industry UsageUsed mainly during the participant recruitment phaseInvolved throughout the clinical trial lifecycle

While Clinical Research Pre Screening focuses on assessing participant eligibility at the start of a study, Clinical Research Coordinators manage the overall conduct of the trial, including recruitment, data collection, and compliance. Both roles are essential but differ in scope and responsibilities within the clinical research process.

What are some common challenges faced by clinical research pre screening professionals, and how can they be addressed?

Clinical Research Pre-Screening professionals often face challenges such as accurately identifying eligible participants from large pools of applicants and ensuring strict adherence to study protocols and regulatory requirements. Managing sensitive patient data and maintaining clear communication with both clinical teams and potential participants can also be demanding. To address these challenges, it's important to stay organized, use standardized screening tools, and participate in regular training on compliance and privacy practices. Collaborating closely with research coordinators and maintaining up-to-date knowledge of study criteria can greatly improve efficiency and accuracy in pre-screening processes.
What are popular job titles related to Clinical Research Pre Screening jobs in Delaware? For Clinical Research Pre Screening jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Clinical Research Pre Screening jobs in Delaware look for? The top searched job categories for Clinical Research Pre Screening jobs in Delaware are:
What cities in Delaware are hiring for Clinical Research Pre Screening jobs? Cities in Delaware with the most Clinical Research Pre Screening job openings:
Clinical Research Pre Screening jobs near you

Field Clinical Advisor - Cell Therapy - Chicago (IL/WI/IN/MN)

AstraZeneca

Wilmington, DE • On-site

$203K - $305K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. FCAs focus on clinical study protocol expertise and education, optimizing the patient journey, and cell therapy pipeline engagement. We are looking for close collaboration with other CTCO Functions, Clinical Development, and Medical Affairs across multiple indications and departments to promote AstraZeneca's diverse cell therapy portfolio.
Summary
Cell Therapy Field Clinical Advisors (FCAs) are part of the Global Cell Therapy Clinical Operations team. They play a critical role in the successful execution of cell therapy clinical trials, driving recruitment, retention, and safety management. Additionally, they allow early insight generation. FCAs focus on clinical study protocol expertise and education, optimizing the patient journey, and cell therapy pipeline engagement. We are looking for close collaboration with other CTCO Functions, Clinical Development, and Medical Affairs across multiple indications and departments to promote AstraZeneca's diverse cell therapy portfolio
You Will:
  • Pipeline mastery at scale: Build knowledge of AstraZeneca's cell therapy pipeline across multiple indications and assets. Convey AstraZeneca's cell therapy strategy, portfolio scope, and product differentiation; ensure compliant messaging across regions.
  • Systematically assess educational needs across owned sites, deliver advanced protocol training, and escalate patterns to Global Clinical Development with recommendations for enterprise solutions.
  • Capture applicable field insights (feasibility, operational bottlenecks, patient pathways) and deliver them to global and local partners to lead early risk identification and inform protocol/process adjustments.
  • Implement targeted protocol education (e.g., inclusion/exclusion criteria application) to lift enrollment rates, reduce screen failures, and minimize attrition.
  • Be the primary field point for protocol and clinical issues-evaluate and escalate, lead root-cause analysis, and implement corrective/preventive actions to reduce deviations and data queries.
  • Insight loop and continuous improvement: Systematically capture site-level insights, summarize trends for study teams and partners, and influence protocol/process adjustments and scaling.
  • Coordinate delivery across CTCO departments, Clinical Development, Medical Affairs, Supply/Logistics, Patient Operations, and Country Ops to ensure rapid, reliable service to partners and study sites.
  • Maintain current knowledge of local regulations, guidelines, codes of practice, and AstraZeneca policies; translate requirements into practical site actions and support inspection readiness.
  • Operate within AZ policies/SOPs and local regulations.
  • Directly improve the speed, quality, and consistency of AstraZeneca's cell therapy trials-reducing cycle times, elevating protocol adherence, and accelerating patient access to innovative treatments.

You Have:
  • Bachelor's degree in a health-related field required; advanced degree (PharmD, PhD, MSc, NP/PA, MD/RN) is preferred.
  • A minimum of 5 plus years in clinical research or field-facing roles within oncology/hematology or advanced therapies; direct cell therapy experience.
  • Concentrated understanding of GCP, clinical trial operations, and cell therapy patient journey
  • Collaboration and Communication: Excellent partner management ability to translate complex protocols into practical site actions.
  • Ability to travel at least 50-80% regionally/nationally and internationally to support sites and program needs.
  • Patient- and site-centric mindset.
  • Data-informed approach to identify trends, risks, and opportunities for operational improvement.

The annual base pay (or hourly rate of compensation) for this position ranges from $203,709 to $305,564 USD. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.
AstraZeneca offers an environment where you can be empowered to make bold decisions and move at pace. With a focus on Oncology, we are driven by speed and backed by leadership that empowers every level to prioritize smart risks based on scientific evidence. Our scale, agility, and passion ensure fast delivery every time. Join us in pioneering new frontiers in cancer research, where courage, curiosity, and collaboration drive patient outcomes. Be part of a team committed to improving the lives of millions with cancer.
Ready to take on this exciting challenge? Apply now to join our dynamic team.
#LI-Remote
Date Posted
04-Aug-2026
Closing Date
30-Aug-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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