Clinical Project Manager, Internal Medicine, IQVIA Biotech
$93.1k - $232.8kIQVIA
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.IQVIA Biotech is seeking an experienced Clinical Project Manager to lead and deliver innovative clinical trials in Internal Medicine. As a Project Manager, you’ll drive operational excellence, manage cross-functional teams, and ensure high-quality delivery that accelerates life-changing therapies to market.Key Responsibilities:Lead global/regional clinical trials from start-up through close-out.Develop and execute study management plans aligned with contract and strategy.Manage timelines, budgets, and risk mitigation across projects.Serve as the primary contact for sponsors and vendors.Ensure compliance with ICH-GCP and regulatory standards.Mentor and support project team members.Qualifications:Bachelor’s degree in Life Sciences or related field preferred.Minimum 5 years of clinical research experience, including 1+ year in project management.Strong therapeutic expertise in Internal Medicine.Proven leadership, communication, and problem-solving skills.Solid understanding of project financials and contract management.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. 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). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.SummaryLocation: Durham, North Carolina, United States of America; San Francisco, CA, United States of America; Collegeville, Pennsylvania, United States of America; Boston, Massachusetts, United States of America; Chicago, Illinois, United States of America; Salt Lake City, UT, United States of America; Kansas City, MO, United States of America; Overland Park, KS, United States of America; New York, NY United States of America; Indianapolis, Indiana, United States of America; Houston, Texas, United States of America; Lexington, KY, United States of America; Parsippany, New Jersey, United States of America; Columbus, Ohio, United States of America; Carlsbad, CA, United States of America; Philadelphia, PA, United States of America; Dallas, Texas, United States of AmericaType: Full time
- ...Senior Clinical Project Manager - Remote, US ICON is a global healthcare intelligence... ...by a mission to bring new medicines and treatments to patients... ...our diverse and dynamic Internal Medicine team. As a Senior... ...in the pharmaceutical or biotech industry. Strong...SuggestedRemote work
- ...Clinical Trial ManagerThe Clinical Trial Manager (CTM) is responsible for the overall operational... ...clinical timelines, enrollment projections, budget tracking, and... ...management.Oversee internal and external clinical study... ...research experience in biotech/pharma, including 2+...SuggestedWork at officeLocal areaFlexible hours
$143.01k - $168.47k
...the right time, in the right way.The Clinical Trial Manager is an experienced clinical operations... ...submissions, health authority inspections, and internal and external audits.Participate in... ..., and drive issue resolution.Strong project management skills with the ability to...SuggestedMinimum wageFull timeWork at officeLocal areaFlexible hours- CSL is seeking a Senior Clinical Trial Case Manager to lead end-to-end case management for global biotechnology and pharmaceutical studies. In this... ...will collaborate closely with investigators, CROs, and internal teams, drive inspection readiness, and mentor junior staff...Suggested
- ...Clinical Research CoordinatorIntegrated Resources, Inc is a premier... ...disorders, and reproductive medicine.Client provides medicines for... ...prevention and treatment), pain management, and women's health. Their... ...individual will Develop strong internal collaboration with...SuggestedLocal areaWorldwide
- ...Senior Local Operations Manager - Oncology - Home... ...healthcare intelligence and clinical research organisation... ...mission to bring new medicines and treatments to... ...for sites, facilitating internal client teaming to drive... ...identified or trends across a project are noted from MVR...Local areaWork visa
- ...\n \n \n Acts as Case Management subject matter expert in cross... ...functional teams for assigned clinical trials. \n \n Manages... ...compliance with national and international regulations, such as GxP guidelines... ...to cross-functional projects to fulfill GxP requirements...Local area
- ...Clinical Operations Lead ICON is a global healthcare intelligence... ...by a mission to bring new medicines and treatments to patients... ...suppliers. As a Clinical Trial Manager at ICON, you will manage... ...with local, national, and international regulations and ethical guidelines...Full timeLocal area
- Clinical Operations Lead ICON plc is a world-leading healthcare intelligence... .... As a Clinical Trial Manager at ICON, you will manage... ...with local, national, and international regulations and ethical guidelines... ...: University degree in medicine, science, or equivalent combination...Local areaFlexible hours
- ...Responsibilities: Ensure efficient, cost-effective clinical trial supply planning and management for low to medium complexity studies Performs... ...or participates in global Clinical Trial Supply project meetings with internal and external team members Partners with R&D...Full timeRelocation package
- ...The Role: Acts as Case Management subject matter expert in cross... ...functional teams for assigned clinical trials. Manages case... ...compliance with national and international regulations, such as GxP guidelines... ...to cross-functional projects to fulfill GxP requirements...Full timeLocal area
- ...Clinical Research Coordinator- McComb, MSICON is a global healthcare intelligence and clinical... ...united by a mission to bring new medicines and treatments to patients faster.As a values... ...protocol deviations, and study outcomes.Managing study-related documentation, including...
- ...Opportunity Details On Assignment Clinical Trial Manager Malvern, Pennsylvania The Clinical Trial Manager (CTM) is responsible for... ...applications (e.g., MS Word and Excel). Skilled at developing project timelines and milestones and working with team to ensure...Shift work
- ...Job Description LAM Senior Clinical Veterinarian or Director... ...rapidly evolving world of genetic medicine. By providing end-to-... ...delivery to meet fast-paced project timelines Compliance and... ...by ACLAM or equivalent international certification ~2 or more years...Full timeTemporary workWorldwide
- ...Senior Clinical Trial Management ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion...Full time
$25 - $36 per hour
About Us Flourish Research is where clinical trials thrive.Flourish Research is one of the industry’s most progressive and diversified... ...CRFs, supplies). Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy. Perform...Hourly payWork at officeMonday to FridayShift work- Flourish Research in Plymouth Meeting, PA is seeking a dedicated clinical research professional to perform protocol-specified patient visits, phlebotomy, and data entry, within an oncology-focused team. The role requires at least two years in clinical research, familiarity...Hourly pay
- Phoenixville Hospital - Tower Health is seeking a candidate to coordinate and facilitate clinical research studies within multidisciplinary teams. The role includes overseeing study activities, processing and shipping specimens, and maintaining study documentation. Qualifications...
- Tower Health is seeking a qualified coordinator for clinical research studies. This role involves facilitating and overseeing research activities in both inpatient and outpatient settings, with a strong emphasis on regulatory document processing and interactions with sponsors...
- CSL Plasma Inc. seeks a Clinical Supply Manager to lead planning and management of clinical trial supplies for low to medium complexity studies. Hybrid onsite in King of Prussia, PA with a minimum of 3 days onsite weekly. Relocation and mobility assistance are not provided...Relocation package
- CSL Behring is seeking a hybrid onsite professional in King of Prussia, PA to manage clinical trial supply planning for low to medium complexity studies. The role requires 5+ years in pharma supply, with strong ICH-GCP and cGMP/cGDP knowledge, and collaboration across R...
- Travel Mt Or Mlt Jobs In Phoenixville, Pa Travel MT or MLT jobs in Phoenixville, PA are available for evening shift assignments with rotating weekends and holiday coverage. You must have strong blood bank experience and be comfortable working as a generalist. Responsibilities...Rotating shiftAfternoon shift
- ...is responsible for obtaining or receiving specimens, performing clinical laboratory tests by standardized procedures, understanding... ...(in partnership with Drexel University). Committed to academic medicine and training, Tower Health offers various programs, including residency...Full timeReliefSummer holidayNight shiftWeekend work
$32 - $36.5 per hour
...Keyboarding experience required;Excellent verbal and written communication skills;One year of clerical experience preferred;One year of clinical experience preferred;Minimum 60 semester hours from a regionally accredited college, including chemistry, biology, and medical...Immediate startFlexible hours- ...quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionTitle: Medical TechnologistDuration: 3+ Months (possible extension)Location...Night shift
- ...release and implantable applications. You will perform pre-formulation studies, characterize drug-polymer interactions using DSC/TGA, and conduct dissolution and degradation testing with HPLC, FTIR, and Raman techniques, contributing to project #J-18808-Ljbffr Secant Group
- Secant Group is seeking an Associate Scientist in Telford, PA to support formulation development and characterization of polymeric materials for biomedical implants and drug-delivery devices. You will conduct pre-formulation studies, perform particle size analysis and microscopy...
$205k - $327.6k
...inspection readiness across global regulations and standards, including FDA, EU MDR, ISO 13485, 21 CFR 820, and other international requirements.Serve as Management Representative and primary interface with global regulatory authorities, including FDA, EU authorities, TGA,...Full timeWork at officeImmediate startWork visa3 days per week$75k - $90k
...to assist in the production and development of vaccines. Assist with endotoxin testing within the lab. Support process improvement projects such as standardization of test methods and the execution of test methods as well as assay validation/qualification. Perform OOS/...- ...integrate and correlate test results with other laboratory data and clinical information. Ability to produce reliable quality laboratory... ..., and typed communication skills. Ability to prioritize and manage numerous tasks simultaneously. Responsible for understanding and...Full timePart timeWork at officeRelocation package2 days per week
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Project Manager, Internal Medicine, IQVIA Biotech. Be the first to apply!
- software implementation project manager Collegeville, PA
- senior implementation project manager Collegeville, PA
- projects Collegeville, PA
- project controls Collegeville, PA
- retail project merchandiser part time Collegeville, PA
- special projects Collegeville, PA
- implementation project manager remote Collegeville, PA
- integrative medicine Collegeville, PA
- sports medicine physician Collegeville, PA
- internal medicine Collegeville, PA



