Associate Principal Scientist, Clinical Research Merck & Co IncAssociate Principal Scientist, Clinical ResearchWest Point, PA$142,400–$224,100 / yearTranslational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients. Leads and directs teams through key study planning, development, and execution activities, including program overviews, issue escalation and mitigation, senior management presentations, cross-functional governance meetings, and advisory meeting preparation.
Clinical Data Manager ZSClinical Data ManagerPhiladelphia, PennsylvaniaAs a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Proven Delivery Leadership: 10+ years of experience leading technology programs in a consulting environment, including direct ownership of scope, staffing, timelines, and delivery outcomes.
NewClinical Trial Manager/Local Delivery Lead GSK plcClinical Trial Manager/Local Delivery LeadPhiladelphia, PA$115,500–$192,500 / yearAgile Thinking, Business Acumen, Clinical Development, Clinical Research, Clinical Research Trials, Clinical Sciences, Clinical Trial Designs, Clinical Trial Development, Clinical Trial Management, Clinical Trial Management Systems (CTMS), Clinical Trial Planning, Clinical Trial Protocols, Clinical Trials, Clinical Trials Operations, Communication, Creativity, Decision Making, Fostering Collaboration, Good Clinical Practice (GCP), Influencing Without Authority, Pharmaceutical Industry, Project Management, Time Management. Leads the local study team consisting of US clinical operations team members, cross functional experts (medical, regulatory, supply logistics, finance, legal, etc.), vendor staff and external clinical site staff involved in study preparation and delivery, providing both matrix leadership and project management of study activities within the United States.
Senior Principal Scientist, Clinical Research, Breast Cancer Merck & Co IncSenior Principal Scientist, Clinical Research, Breast CancerNorth Wales, PA$282,200–$444,200 / yearMonitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs; Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and. Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.
Clinical Trial Supply (CTS) Study Manager CSL Behring LLCClinical Trial Supply (CTS) Study ManagerKing of Prussia, PAWe use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
2027 Future Talent Program - Diversity and Inclusion in Clinical Trials (DICT) - Intern Merck & Co Inc2027 Future Talent Program - Diversity and Inclusion in Clinical Trials (DICT) - InternNorth Wales, PA$39,908–$111,111 / yearThis internship provides a unique opportunity to contribute to initiatives that help ensure clinical trials reflect the diverse populations impacted by disease and treatment outcomes. During the 12-week internship program, the intern will support one or more high-impact projects focused on identifying and addressing barriers to clinical trial participation among underrepresented populations.
Director, Clinical Data Management, Digital Health Technologies, Hybrid Merck & Co IncDirector, Clinical Data Management, Digital Health Technologies, HybridNorth Wales, PA$173,200–$272,600 / yearRequired Skills: Clinical Data Management, Data Validation, Decision Making, Digital Technology, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), People Leadership, Results-Oriented, Strategic Thinking, Support Management, System Improvements, Vendor Management. Experience working with internal (Clinical Sciences, BARDS, Global Clinical Trial Operations (GCTO), our Research & Development Division IT) and external (functional service providers, labs, investigator sites, etc.) stakeholders to deliver products and services supporting a portfolio of clinical trials/programs across multiple therapeutic areas.
Senior Principal Scientist, Clinical Research, Thoracic Malignancies Merck & Co IncSenior Principal Scientist, Clinical Research, Thoracic MalignanciesNorth Wales, PA$282,200–$444,200 / yearMonitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs; Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and. Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.
Financial Analyst, Clinical Trials - Fox Chase Cancer Center Temple University Health SystemFinancial Analyst, Clinical Trials - Fox Chase Cancer CenterPhiladelphia, PAThis includes the development of clinical research budgets (from start to finish); budget amendments; budget negotiations; creating reports; reviewing clinical trial agreements; scientific protocol, and maintaining fee schedule updates. Responsible for financial and accounting processes and deliverables related to clinical research activities invoicing & large data sets.
Associate Director, Clinical Pharmacology Modeling and Simulation Oncology GSK plcAssociate Director, Clinical Pharmacology Modeling and Simulation OncologyCollegeville, PA$147,675–$246,125 / yearArtificial Intelligence (AI), Clinical Development, Clinical Pharmacology, Drug Development, Drug Discovery Research, In Vitro Models, Modeling Simulations, Nonlinear Mixed Effects Modeling (NONMEM), NONMEM, Oncology, Pharmaceutical Sciences, Pharmacodynamics, Pharmacokinetics, Pharmacometrics, Regulatory Compliance. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.
Principal Scientist, Biostatistics, Late-Stage Clinical Development Merck & Co IncPrincipal Scientist, Biostatistics, Late-Stage Clinical DevelopmentNorth Wales, PA$190,800–$300,300 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company Research Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine projects.
Inpatient Clinical Denial Specialist - FT - Day - Revenue Integrity & Denials Mgmt Lawrenceville NJ Capital HealthInpatient Clinical Denial Specialist - FT - Day - Revenue Integrity & Denials Mgmt Lawrenceville NJNJ$20.10–$26.13 / hourOther Credentials: Knowledge and Skills: Working knowledge of inpatient clinical denial categories, including medical necessity, patient status, and readmissions Familiarity with utilization review processes and clinical documentation workflows Ability to perform detailed tracking, documentation, and inventory management across multiple appeal levels Strong organizational skills and attention to detail Ability to identify root causes and recurring denial drivers Strong written communication skills for documentation and internal coordination Proficiency with hospital billing systems, EMR navigation, and payer portals Proficiency with Microsoft Office applications, including Excel. Ensures inpatient clinical denial cases are properly triaged, routed, documented, tracked, and prepared for appeal in accordance with payer requirements, while partnering with clinical and operational resources to support timely resolution and denial prevention.
Senior Application Analyst - IS Clinical Systems Training and Education University Health Services IncSenior Application Analyst - IS Clinical Systems Training and EducationKING OF PRUSSIA, PAThe Senior Application Analyst - IS Clinical Systems Training and Education provides learning and development services to UHS Corporate, acute care, and behavioral health facilities to increase the effectiveness of clinical and technical staff and ensure the delivery of quality healthcare services to our patients. Operating acute care hospitals, behavioral health facilities, outpatient facilities and ambulatory care access points, an insurance offering, a physician network and various related services located in 40 U.S. states, Washington, D.C., Puerto Rico and the United Kingdom.
Clinical Research Project Manager A/B University of PennsylvaniaClinical Research Project Manager A/BPA$63,085–$89,789 / yearWith mentoring from the Principal Investigator and Associate Director, the Clinical Research Project Manager A/B will take a leadership role in developing study protocols, managing the detailed operations of projects, coordinating activities in single center and/or multi-center studies, assisting with quality control, and assisting with grant applications when applicable. Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility.
Outpatient Clinical Denial Specialist - FT - Day - Revenue Integrity & Denials Mgmt Lawrenceville NJ Capital HealthOutpatient Clinical Denial Specialist - FT - Day - Revenue Integrity & Denials Mgmt Lawrenceville NJNJ$20.10–$26.13 / hourOther Credentials: Knowledge and Skills: Working knowledge of outpatient clinical denial categories, including payer medical policy, experimental/investigational, and clinical criteria denials Familiarity with payer authorization processes and outpatient clinical documentation workflows Ability to perform detailed tracking, documentation, and inventory management across multiple appeal levels Strong organizational skills and attention to detail Ability to identify root causes and recurring outpatient denial drivers Strong written communication skills for documentation and internal coordination Proficiency with hospital billing systems, EMR navigation, and payer portals. Ensures outpatient clinical denial cases are properly triaged, routed, documented, tracked, and prepared for appeal in accordance with payer requirements, while partnering with clinical and operational resources to support timely resolution and denial prevention.
Clinical Dietitian Coordinator Main Line Health SystemClinical Dietitian CoordinatorMalvern, PA$34.96–$54.16 / hourIn addition to clinical responsibilities, the Lead Dietitian devotes approximately 20% of their role to providing administrative and staff support to Clinical Nutrition Manager (CNM), contributing to departmental operations, staff coordination, and quality initiatives. The Lead Dietician functions as an integral member of the multidisciplinary healthcare team, collaborating to develop, coordinate, implement, and assess individualized nutrition care plans that support optimal patient outcomes.
NewTrauma Clinical Nurse Coordinator, Full Time, 7a-3:30p Temple University Health SystemTrauma Clinical Nurse Coordinator, Full Time, 7a-3:30pPhiladelphia, PA407583'',''true'',''407583'',''false'',''Submission for the position: Trauma Clinical Nurse Coordinator, Full Time, 7a-3:30p - (Job Number: 264682)'',''false'',''407583'',''false'',''true'',''Trauma Clinical Nurse Coordinator, Full Time, 7a-3:30p'',''264682'',''!*!Collaborates with the Trauma Director and Trauma Program Manager on clinical components of the Trauma Program. '',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Nursing'',''Nursing'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''407583'',''407583'',''true'',''407583'',''false'',''Submission for the position: Trauma Clinical Nurse Coordinator, Full Time, 7a-3:30p - (Job Number: 264682)'',''false'',''407583'',''false'',''true''.
2027 Future Talent Program -Global Clinical Trial Operations (GCTO) Project Management Office (PMO) - Intern PMO Intern Merck & Co Inc2027 Future Talent Program -Global Clinical Trial Operations (GCTO) Project Management Office (PMO) - Intern PMO InternNorth Wales, PA$39,908–$111,111 / yearThe intern will engage with the Project Management Office (PMO) organization and their associated project teams throughout participation in and/or leadership of initiatives that drive the efficient and ethical conduct of clinical trials across GCTO. Required Education and Skills: Candidates must be currently enrolled in a full-time BS/BA degree program in a business or project management, continuous improvement, computer technology, or science related discipline.
2027 Future Talent Program - Clinical Business Operations - Intern Merck & Co Inc2027 Future Talent Program - Clinical Business Operations - Internupper gwynedd, PA$39,908–$111,111 / yearClinical Data Management is the practice of defining, designing, implementing, investigating, cleaning end ensuring that data collected in support of the needs of a clinical research trial satisfy the analysis and reporting requirements necessary to satisfy (regulatory requirements) of the planned Clinical Study Report. Business Operations supports the GDMS organization in the areas of Portfolio & Resource Operations, Project Management, Change Management, Communications, Learning & Development and Metrics/KPIs.
2027 Future Talent Program - Leveraging Advanced Analytics and Automation to Enhance Clinical Bioanalytical Operations - Intern Merck & Co Inc2027 Future Talent Program - Leveraging Advanced Analytics and Automation to Enhance Clinical Bioanalytical Operations - Internlower gwynedd township, PAActivities may include analyzing assay performance trends, developing automated data processing tools, evaluating laboratory workflows, and generating insights that support clinical assay operations. This internship provides an opportunity to work alongside scientists supporting global clinical development programs while gaining experience in regulated environments and modern bioanalytical technologies.