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Clinical Jobs in Bainbridge, MD

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Clinical Trial Assistant, HYBRID in Wilmington, DE IQVIA

Wilmington, Delaware

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

30+ days ago

Clinical Research Technologist Nemours Foundation

Wilmington, DE

Responsibilities include: Receives biospecimens from the LHC collection sites into the ALA-ACRC biorepository housed at Nemours Biobank and Molecular Analysis Program (BMAP), which includes tracking incoming shipments, accepting shipments, cataloging shipment biospecimens, completing paperwork and computer entry related to acquisition. This individual will manage receipt and storage of biospecimens from the (LHC) American Lung Association Airways Clinical Research Center network (ALA-ACRC) sites and other ALA-ACRC studies as required.

30+ days ago

Clinical Research Associate (CRA II/Senior) - Metabolic - US Any Region Parexel International Corp

With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.

30+ days ago

Clinical Research Technologist II- Biobank Nemours Foundation

Wilmington, DE

Essential Functions: Responsible for processing various biological specimens (blood and body fluid, tissue, bone marrow, etc.) and utilizing databases for specimen tracking and storage, following laboratory protocols and SOP's. This individual will conduct routine specimen processing and shipping for both internally and externally funded projects of interest to the laboratory, including plasma/serum processing, mononuclear cell extraction, tissue culture, specimen data entry, and accessioning.

30+ days ago

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Newark, DE

$74,500–$197,500 / year

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

20 days ago

Senior Clinical Research Associate Alexion Pharmaceuticals Inc

Wilmington, DE

CRA works in close collaboration with (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. CRA is responsible for the selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

30+ days ago

Clinical Applications Programmer II Pharmaron

Baltimore, MD

$60,000–$70,000 / year
Full time
Quick Apply

Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. Position: Clinical Applications Programmer IISalary Range: $60,000-70,000Location: Baltimore, MDAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life.

30+ days ago

Senior Clinical Trial Manager Incyte Corp

Wilmington, DE

Job Summary Primary Function The Sr Clinical Trial Manager provides input to the overall operational trials implementation manages trials timelines budget feasibility country identification and sites selection enhanced patient recruitment functions as the primary liaison for internal stakeholders and vendors leads multidisciplinary departments initiatives and provides support for process changes to increase efficiency in study executions. Through the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia.

17 days ago

Senior Clinical Project Manager ClinChoice

Romania, PA

Remote

Key words: Senior Project Manager, Senior Clinical Project Manager, Senior Study Manager, Senior Clinical Trial Manager, Study Management, Project Management, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Study Management, Project Leader, Project Lead, complex clinical trials, oncology, respiratory, CRO, Contract Research Organization. In this role, you will lead cross-functional teams and oversee the execution of complex clinical trials, ensuring successful delivery in accordance with contractual commitments, SOPs, ICH-GCP guidelines, and applicable regulatory requirements.

26 days ago

Research Coordinator - Clinical Trials Unit Kennedy Krieger Institute

Baltimore, Maryland

2. Under the direction of the Senior Research Coordinator, assist and support daily clinical trial and research study activities, including participant recruitment and scheduling, study procedure scheduling and coordination, obtaining results and ensuring clinician review, and documentation completion. Overview: The Research Coordinator assists and collaborates with the Principal Investigator (PI) and research collaborators for research studies related to neurological, neurogenetic neurodevelopmental and psychiatric conditions in children, adolescents, and adults.

30+ days ago

Research Coordinator Clinical Trials Unit Kennedy Krieger Institute Inc

Baltimore, MD

Under the direction of the Senior Research Coordinator, assist and support daily clinical trial and research study activities, including participant recruitment and scheduling, study procedure scheduling and coordination, obtaining results and ensuring clinician review, and documentation completion.3. The Research Coordinator assists and collaborates with the Principal Investigator (PI) and research collaborators for research studies related to neurological, neurogenetic neurodevelopmental and psychiatric conditions in children, adolescents, and adults.

30+ days ago

Clinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations Nationwide Headlands Research

Baltimore, MD

$45,000–$100,000 / year

This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.

30+ days ago

Clinical Research Assistant Nemours Foundation

Wilmington, DE

The job includes but is not limited to: screening patients for study eligibility, scheduling research visits/follow up, tracking/auditing consent forms and study related documents, preparation for both internal and external audits, collecting data and submitting to appropriate organizations, processing/packaging of lab specimens, maintaining inventory of research supplies, creating electronic research charts, scheduling site monitor visits and meeting rooms as needed and assisting in the implementation of new laboratory protocols and processes. The Clinical Research Assistant will be required to complete Human Subjects Protection (HSP) training, CITI training (including Good Clinical Practice (GCP), as well as become a member of the Children's Oncology Group (COG) research base.

21 days ago

Part-time or Full-time Physician - Clinical Research Headlands Research Inc

Baltimore, MD

Pharmasite Research, located in the greater Baltimore area, is a dedicated clinical research site with over twenty years of experience across multiple therapeutic areas, with a particular focus on mental health and central nervous system (CNS) conditions. With an experienced team serving a diverse population, Pharmasite Research partners with sponsors and CROs to advance innovative therapies and improve health outcomes.

30+ days ago

Clinical Trial Manager Prelude Therapeutics

Wilmington, DE

Contribute to the development, review and approval of study documents including but not limited to protocol, ICF, multiple clinical trial plans, EDC/CRFs, pharmacy manual, oversight manuals, clinical study reports, patient narratives and Clinical Trial Agreements (Clinical and Legal review). Provide strategic clinical trial input related to study logistics, management and oversight of enrollment (including forecasting), clinical supply and drug supply, data review and data cleaning and Trial Master Files.

6 days ago

Provider Clinical Operations Consultant, Manager PricewaterhouseCoopers LLP

Baltimore, MD

$99,000–$232,000 / year

Preference for at least one of the following fields of study: Accounting, Actuarial Science, Analytics/Data Science, Business Administration/Management, Computer Science/Information Systems, Economics, Engineering, Finance, Government/Public Policy, Health Administration/Public Health, Mathematics/Statistics, Operations/Supply Chain, Organizational Management/Behavior, Risk Management/Insurance. As a Provider Clinical Operations Consultant, Manager you will lead client service workstreams focused on provider clinical operations, bringing together operations consulting methods, health services knowledge, and process improvement skills to support clinical modernization efforts within our Operations Consulting practice.

16 days ago

RN I Clinical Research Medical Oncology Hematology Consultants

Middletown, Delaware

Our board-certified physicians in Hematology and Medical Oncology, Palliative Care Medicine, and breast surgery have trained and held faculty positions in nationally and internationally recognized academic centers. We are affiliated with the US Oncology Network, which is one of the nation’s largest networks of integrated, community-based oncology practices that are dedicated to advancing high-quality, evidence-based cancer care.

21 days ago

Clinical Data AMS Sr. Consultant Deloitte

Baltimore, MD

$120,200–$140,000 / year

This role owns the health, stability, and compliance posture of a suite of clinical and regulatory R&D platforms - including Axway Secure Transport (ST), eClinical Elluminate, Eclipse (medical coding), and EAST - across the full engagement lifecycle: implementation, configuration, validation, and steady-state managed services. The team operates at the intersection of IT infrastructure, clinical operations, and quality/regulatory compliance, partnering closely with global business and technology stakeholders to support end-to-end clinical trial data lifecycles from data capture and coding through statistical analysis and submission-ready outputs.

3 days ago

Clinical Trial Assistant, HYBRID in Wilmington, DE IQVIA Holdings Inc

Wilmington, DE

$35,800–$123,000 / year

30+ days ago

Clinical Applications Programmer II Pharmaron Beijing Co Ltd

Baltimore, MD

$60,000–$70,000 / year

Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. Bachelor's degree/equivalency (120+ college credit hours) plus 1 year of relevant experience in at least two of the following areas: Clinical research, life sciences, public health, or related field.

30+ days ago

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Clinical Jobs in Bainbridge, MD

Clinical Trial Assistant, HYBRID in Wilmington, DE IQVIA

Clinical Research Technologist Nemours Foundation

Clinical Research Associate (CRA II/Senior) - Metabolic - US Any Region Parexel International Corp

Clinical Research Technologist II- Biobank Nemours Foundation

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Senior Clinical Research Associate Alexion Pharmaceuticals Inc

Clinical Applications Programmer II Pharmaron

Senior Clinical Trial Manager Incyte Corp

Senior Clinical Project Manager ClinChoice

Research Coordinator - Clinical Trials Unit Kennedy Krieger Institute

Research Coordinator Clinical Trials Unit Kennedy Krieger Institute Inc

Clinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations Nationwide Headlands Research

Clinical Research Assistant Nemours Foundation

Part-time or Full-time Physician - Clinical Research Headlands Research Inc

Clinical Trial Manager Prelude Therapeutics

Provider Clinical Operations Consultant, Manager PricewaterhouseCoopers LLP

RN I Clinical Research Medical Oncology Hematology Consultants

Clinical Data AMS Sr. Consultant Deloitte

Clinical Trial Assistant, HYBRID in Wilmington, DE IQVIA Holdings Inc

Clinical Applications Programmer II Pharmaron Beijing Co Ltd

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