1,394 Results for

Clinical Research Jobs in Lawndale, PA

Jobs

King of Prussia, PA

p>To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/. We 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.

3 days ago

Remote

$97,000–$193,000 / year

li>

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

16 days ago

Blue Bell, PA

Remote

Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role.

30+ days ago

Blue Bell, PA

p>Our benefits examples include:

• Various annual leave entitlements • A range of health insurance offerings to suit you and your family's needs • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

30+ days ago

Wilmington, DE

The CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Clinical Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner on a site level.

Following quality issue processes by escalating systematic or serious quality issues, data privacy breaches, or ICH-GCP compliance issues to Global Study team, Local study team, Country Operations Line Management and/or Quality Group, representatives as required.

10 days ago

Philadelphia, PA

Remote

$105,000–$115,000 / year

o Identification of data discrepancies and compliance concerns, present findings to site research staff, provide retraining if needed, provide problem-solving strategies and communicate findings to the study team and department management via escalation of issues and/or within the monitoring visit report. Our current Interventional products include a broad range of clinically relevant solutions, such as our GuideLiner and Turnpike Catheters, Ringer Perfusion Balloon Catheter, AC3 Optimus and AC3 Range Intra-Aortic Balloon Pumps and the OnControl Powered Bone Access System.

30+ days ago

Princeton, NJ

Remote

SystImmune currently has multiple assets in clinical development across solid tumor and hematologic malignancies, supported by a robust preclinical pipeline advancing novel oncology therapeutics through discovery and IND-enabling stages.

The ideal candidate is a highly organized, self-motivated clinical operations professional with strong oncology monitoring experience who can work independently while collaborating effectively with cross-functional teams and external vendors.

12 days ago

Blue Bell, TX

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

30+ days ago

Princeton, NJ

$90,000–$130,000 / year

Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.

30+ days ago

Princeton, NJ

$90,000–$130,000 / year

li>Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. CRA is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.

1 day ago

li>

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Bonus, Com, Stock, Benefits & Disclaimer verbiage:
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level.

30+ days ago

Blue Bell, PA

Collaborating with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of clinical trials. You will be a key contributor to the success of clinical trials by driving site performance, providing mentorship to CRAs, and ensuring the highest levels of data quality and patient safety.

30+ days ago

Blue Bell, PA

p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

5 days ago

Plainsboro Township, New Jersey

$115,000–$130,000 / year

Train and support external trial staff regarding CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability, temperature monitoring, query resolution, essential document collection, and ITF filing. Collaborate with Local Trial Manager (LTM) and Line of Business Manager, communicating site progress and escalating critical issues impacting trial milestones.

30+ days ago

Cherry Hill, New Jersey

li>Develop and deliver technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.

Assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices), PHI (Personal Health Information) and regulatory requirements.

10 days ago

Cherry Hill, New Jersey

10 days ago

Blue Bell, TX

Key responsibilities include: Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.

23 days ago

Blue Bell, PA

p>Key responsibilities include:

Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.

8 days ago

Princeton, NJ

Remote

Full time

6 days ago

Princeton, New Jersey

li style="width:6.6493in">Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites.

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ.

25 days ago

North Wales, PA

$282,200–$444,200 / year

Required Skills: Clinical Development, Clinical Judgment, Clinical Medicine, Clinical Research Management, Clinical Sciences, Clinical Trial Development, Clinical Trials, Drug Development, Intellectual Curiosity, Oncology, Oncology Research, Pharmaceutical Development, Strategic Planning. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area.

30+ days ago

$282,200–$444,200 / year

p>The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section.

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.

30+ days ago

Philadelphia, PA

p>''404090'',''true'',''404090'',''false'',''Submission for the position: Clinical Research Integrity Coordinator - (Job Number: 262721)'',''false'',''404090'',''false'',''true'',''Clinical Research Integrity Coordinator'',''262721'',''!*!The Research Quality Assurance Analyst reviews the requirements necessary for attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level.

'',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Research & Science'',''Research & Science'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''404090'',''404090'',''true'',''404090'',''false'',''Submission for the position: Clinical Research Integrity Coordinator - (Job Number: 262721)'',''false'',''404090'',''false'',''true''.

9 days ago

Marlton, NJ

$60,000–$75,000 / year

Make all the arrangements for periodic meetings, such as Physician Adjudication Committees, Data Safety Monitoring Boards, and Monthly Webcast meetings, and assist the Clinical Trial Manager with the preparation of the meetings.

Manage and organize all administrative aspects for assigned clinical trials, including creation and maintenance of site personnel contact information, mass mailings, study regulatory documents, and electronic or binder preparation for distribution.

30+ days ago

Philadelphia, PA

Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team. 1 year experience in a health care environment as a Clinical Research Associate, Clinical Research Coordinator Clinical research Nurse or Medical Chart Auditor Required.

9 days ago

Princeton, NJ

$80,000–$110,000 / year

Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).

30+ days ago

Philadelphia, PA

Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team. 5 years experience in a health care environment as a Clinical Research Associate, Clinical Research Coordinator, Clinical Research Nurse or Medical Chart Auditor Required.

30+ days ago

Philadelphia, PA

$58,300–$72,900 / year

CRCII works closely with PIs and study Sponsors to complete study start-up activities, oversee patient enrollment and ensure all research visits are performed according to protocol. Led by experts in in vivo gene therapy research, with more than 10 years of clinical trial experience, the CIGT team has a wealth of knowledge to navigate the complex safety, regulatory, and clinical care considerations of gene therapy clinical research.

4 days ago

Philadelphia, PA

$51,730–$64,660 / year

Additional responsibilities include screening potential research participants and clinical patients for enrollment; scheduling and completing participant visits and collecting biospecimen samples (visits may occur on CHOP main campus, at external satellite sites or in the community); consenting participants and research families for enrollment; performing routine email and phone follow-up with consented families who have outstanding study-related tasks. A Clinical Research Coordinator position is open as part of a new large-scale longitudinal project spanning multiple departments (Developmental Behavioral Pediatrics, Neurology, Genetics, Center for Autism Research) at the Children's Hospital of Philadelphia.

25 days ago

Philadelphia, PA

$22.61–$28.26 / hour

Led by experts in in vivo gene therapy research, with more than 10 years of clinical trial experience, the CIGT team has a wealth of knowledge to navigate the complex safety, regulatory, and clinical care considerations of gene therapy clinical research. The Clinical In Vivo Gene Therapy group (CIGT) is dedicated to developing and conducting adeno-associated virus gene transfer and molecular therapy trials at Children's Hospital of Philadelphia.

18 days ago

Philadelphia, Pennsylvania

$50,000–$55,000

The Clinical Research Coordinator works under the leadership of the Principal Investigator and/or other Research Staff and is responsible for specific research tasks associated with clinical research projects or clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study operations. Coordinators who successfully earn industry-recognized certifications, such as the Certified Clinical Research Professional (CCRP®) through SOCRA or the Certified Clinical Research Coordinator (CCRC®) through ACRP, may qualify for advancement sooner.

30+ days ago

Philadelphia, Pennsylvania

$50,000–$55,000

30+ days ago

Philadelphia, Pennsylvania

$50,000–$55,000

30+ days ago

Princeton, New Jersey

li style="margin-left:8px">Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites.

Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).

30+ days ago

Philadelphia, PA

Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team. In addition, this position is expected to interact with the institutional investigators, other members of healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.

4 days ago

Philadelphia, PA

Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team. In addition, this position is expected to interact with the institutional investigators, other members of healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.

9 days ago

North Wales, PA

$255,800–$402,700 / year

The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.

30+ days ago

Upper Gwynedd, PA

$255,800–$402,700 / year

p>The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.
The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the ophthalmology therapeutic area.

24 days ago

$255,800–$402,700 / year

p>The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.
The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section.

30+ days ago

Philadelphia, PA

$51,730–$64,660 / year

Under moderate supervision from study PI or other research study management staff, this role provides substantial coordination level support for all clinical research activities within the scope of clinical research protocols. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine.

25 days ago

Philadelphia, PA

Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team. In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.

11 days ago

Blue Bell, CT

What You Will Be Doing: • Serve as the primary point of contact between investigational sites and the sponsor • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out • Ensure site compliance with ICH-GCP, SOPs, and regulations • Maintain up-to-date documentation in CTMS and eTMF systems • Support and track site staff training and maintain compliance records • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting • Support subject recruitment and retention efforts at the site level • Oversee drug accountability and ensure proper storage, return, or destruction • Resolve data queries and drive timely, high-quality data entry • Document site progress and escalate risks or issues to the clinical team • Assist in tracking site budgets and ensuring timely site payments (as applicable) • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs. You Are: A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RNE Eligible to work in United States without visa sponsorship A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry Experience monitoring Oncology studies Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF A clear communicator, problem-solver, and collaborative team player Willing and able to travel up to 50% for on-site monitoring visits across northeast region; preference given to candidates residing in Connecticut near major HUB airports to support efficient regional travel.

30+ days ago

Camden, NJ

p>• 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.

30+ days ago

Philadelphia, PA

p>''402895'',''true'',''402895'',''false'',''Submission for the position: CLINICAL RESEARCH NURSE II - (Job Number: 262232)'',''false'',''402895'',''false'',''true'',''CLINICAL RESEARCH NURSE II'',''262232'',''!*!Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated.

'',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Nursing Admin & Management'',''Nursing Admin & Management'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''402895'',''402895'',''true'',''402895'',''false'',''Submission for the position: CLINICAL RESEARCH NURSE II - (Job Number: 262232)'',''false'',''402895'',''false'',''true''.

9 days ago

West Point, PA

$142,400–$224,100 / year

p>Translational 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.

3 days ago

$310,900–$489,400 / year

li>

Working closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility.

Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.

30+ days ago

North Wales, PA

$310,900–$489,400 / year

li>

30+ days ago

Philadelphia, PA

$47,313–$53,418 / year

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. The clinical research coordinator will be held responsible for all aspects of study coordination including subject recruitment, detailed data entry, collecting biospecimens, subject visits and follow-up and regulatory documentation.

24 days ago

Philadelphia, PA

$47,313–$53,418 / year

30+ days ago

Philadelphia, PA

9 days ago

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Clinical Research Jobs in Lawndale, PA

Auditor - GCP CSL Behring

Senior Clinical Research Associate - Cardio - East Coast - Remote Worldwide Clinical Trials Holdings Inc

Senior Clinical Research Associate ICON Plc

Clinical Research Associate ICON Plc

Clinical Research Associate Alexion Pharmaceuticals Inc

Regional Clinical Research Associate (REMOTE) Teleflex Inc

Senior Clinical Research Associate-Contractor Systimmune Inc

Clinical Research Associate II ICON Plc

Senior Clinical Research Associate Systimmune Inc

Sr. Clinical Research Associate Systimmune Inc

Sr. Clinical Research Associate ICON Plc

Lead Clinical Research Associate ICON Plc

Senior Clinical Research Associate - East Coast ICON Plc

Senior Clinical Research Associate System One

Senior Clinical Research Associate 6942-ABIOMED Legal Entity

Senior Clinical Research Associate Johnson & Johnson

Clinical Research Associate I ICON Plc

Clinical Research Associate, Histologist ICON Plc

Senior Clinical Research Associate-Contractor Systimmune

Sr. Clinical Research Associate Systimmune

Senior Clinical Director (Senior Principal Scientist), Clinical Research, RCC Merck & Co Inc

Senior Clinical Director, Clinical Research, Hematology Merck & Co Inc

Clinical Research Integrity Coordinator Temple University Health System

Clinical Research Associate Impulse Dynamics Germany GmbH

Clinical Research Integrity Coordinator Temple Health

Clinical Research Associate II Systimmune Inc

Senior Clinical Research Integrity Coordinator Temple Health

Clinical Research Coordinator II - Clinical In Vivo Gene Therapy (CIGT) Children's Hospital of Philadelphia

Clinical Research Coordinator I - Profound Autism Research Study Children's Hospital of Philadelphia

Clinical Research Assistant II- The Clinical In Vivo Gene Therapy Group Children's Hospital of Philadelphia

Clinical Research Coordinator-Katz Temple University

Clinical Research Coordinator-Recruitment Temple University

Clinical Research Coordinator Temple University

Clinical Research Associate II Systimmune

Clinical Research Nurse (Phase 1) Temple Health

Clinical Research Nurse II Temple Health

Clinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co Inc

Clinical Director, Clinical Research, Ophthalmology Merck & Co Inc

Clinical Director, Clinical Research, Hematology Merck & Co Inc

Clinical Research Coordinator I - PolicyLab Clinical Futures Children's Hospital of Philadelphia

Extramural Clinical Research Coordinator Temple Health

Clinical Research Associate - Oncology - Connecticut ICON Plc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

CLINICAL RESEARCH NURSE II Temple University Health System

Associate Principal Scientist, Clinical Research Merck & Co Inc

Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma Merck & Co Inc

Executive Director, Product Development Team Leader, Clinical Research, Hematology Merck & Co Inc

Clinical Research Coordinator A/B (Pregnancy & Perinatal Research Center) University of Pennsylvania

Clinical Research Coordinator A/B (OBGYN - Pregnancy & Perinatal Research Center University of Pennsylvania

Clinical Research Integrity Coordinator Fox Chase

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