747 Results for

Clinical Research Associate Jobs in Camden, NJ

Jobs

New!

Princeton, NJToday

$23–$27 Per Hour

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.

Perform functionality testing on devices and support group scientists with device assembly and testing.

New!

Philadelphia, PA6 days ago

Remote

$153,541–$230,312 Per Year

Build, maintain, and evolve operational, unit-based forecasts across the portfolio – demand, revenue, and patient-based models – including scenario planning and risk and opportunity assessments for multiple launches and in-line products.

New!

Philadelphia, PA6 days ago

$153,541–$230,312 Per Year

li>The current base salary range for this position is expected to be between $153,541 and $230,312 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Our team’s proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities.

New!

Philadelphia, PA6 days ago

Remote

$153,000–$230,000 Per Year

Operating at the intersection of strategy and execution, this role partners closely with cross-functional colleagues and external experts to deliver high‑impact publications and scientific communications that advance both patient care and scientific dialogue.

The current base salary range for this position is expected to be between $153,000 and $230,000 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.

Blue Bell, PA30+ days ago

Remote

Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

Philadelphia, PA30+ days ago

Remote

$105,000–$115,000 Per 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.

Plainsboro Township, New Jersey30+ days ago

$115,000–$130,000 Per 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.

Cherry Hill, New Jersey7 days ago

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.

PA13 days ago

Remote

$97,000–$193,000 Per Year

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.

Princeton, New Jersey30+ days ago

We will assess the specific title and level of entry during the interview and assessment process since the actual salary offer will be based on a number of factors, including but not limited to the candidate’s qualifications, experience, skills, and competencies for the role. As a Clinical Research Associate with experience managing clinical trial sites, the number years and type of monitoring experience will determine CRA level.

Cherry Hill, New Jersey7 days ago

Wilmington, DE7 days ago

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.

Blue Bell, PA30+ days ago

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.

Blue Bell, TX30+ days ago

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.

CA30+ days ago

$110,520–$138,150 Per Year

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.

New!

Blue Bell, PA2 days ago

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.

Blue Bell, PA30+ days ago

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.

Princeton, NJ9 days ago

Remote

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.

Princeton, NJ30+ days ago

$90,000–$130,000 Per 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.

New!

Princeton, NJ6 days ago

$90,000–$130,000 Per 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.

New!

Princeton, NJ3 days ago

Remote

Full-time

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.

Princeton, NJ30+ days ago

Full-time

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.

Blue Bell, PA20 days ago

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.

New!

Blue Bell, PA5 days ago

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.

Marlton, NJ30+ days ago

$60,000–$75,000 Per 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.

Princeton, NJ30+ days ago

$80,000–$110,000 Per 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).

Princeton, NJ30+ days ago

Full-time

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. The CRA II 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.

Camden, NJ30+ days ago

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.

Blue Bell, CT30+ days ago

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.

Philadelphia, Pennsylvania30+ days ago

$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.

Philadelphia, Pennsylvania30+ days ago

$50,000–$55,000

Philadelphia, Pennsylvania30+ days ago

$50,000–$55,000

New!

Philadelphia, PA6 days ago

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'',''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''.

Philadelphia, PA30+ days ago

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.

New!

Philadelphia, PA6 days ago

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.

Philadelphia, PA30+ days ago

$52,500–$53,418 Per Year

p>The Clinical Research Coordinators will be responsible for day-to-day study coordination and operations of the medical marijuana study and projects within the CAIML Lab such as (i) a study involving the use of a clinical decision support system for older adults in primary care clinics to promote diagnostic excellence, and (ii) a study investigating the preferences and tradeoffs among primary care patients and clinicians associated with AI electronic consultations. The research coordinators will have responsibilities that span across two areas: 1) driving the implementation of a study to understand the impact of medical marijuana on quality of life for patients with advanced cancer and 2) supporting Dr. Gary Weissman's team, the Clinical Artificial Intelligence and Machine Learning (CAIML) Lab.

Philadelphia, PA27 days ago

Duties include identifying patients appropriate for participation, consenting patients for database/repository participation, overseeing collection and processing of blood and tissue specimens, managing the biorepositories, including associated databases, compiling data and assisting with writing of various research documents, and maintaining metrics of collection to these repositories. The GI Oncology Clinical Research team, located within the Abramson Cancer Center of the University of Pennsylvania and comprised of faculty in the Division of Hematology and Oncology, is seeking a Clinical Research Coordinator (CRC) under direct supervision, to assist with recruitment to and maintenance of biospecimen based GI cancer repositories.

Philadelphia, Pennsylvania9 days ago

5501 Old York Road, Philadelphia, Pennsylvania, United States of AmericaNationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value. Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research.

New!

Philadelphia, PA6 days ago

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.

Philadelphia, PA30+ days ago

Wilmington, DE30+ days ago

Full-time

Nemours is seeking a Clinical Research Coordinator to join our Nemours Children's Health team in Wilmington, DE.The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or clinical trials in the Orthogenetics Department at Nemours Children's Hospital Delaware by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.

Philadelphia, PA30+ days ago

Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.

Philadelphia, PA22 days ago

$51,730–$64,660 Per 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.

Philadelphia, PA30+ days ago

$47,313–$53,418 Per 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.

Philadelphia, PA21 days ago

$47,313–$53,418 Per Year

Philadelphia, Pennsylvania30+ days ago

$45,000–$45,000

The Clinical Research Assistant works under the direct supervision of the Principal Investigator and/or other Research Coordinators and will assist with specific research tasks associated with clinical research projects or clinical trials. With access to advanced resources, collaborative teams, and a strong commitment to excellence, Temple offers an ideal environment for Clinical Research Coordinators to grow their careers while shaping the future of medicine.

Philadelphia, PA30+ days ago

Work ShiftWorkday Day (United States of America)Worker Sub TypeRegularEmployee EntityThomas Jefferson UniversityPrimary Location Address901 Walnut Street, Philadelphia, Pennsylvania, United States of AmericaNationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value. Job DescriptionOversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).Trains and supervises research staff on the proper procedures for conducting a clinical trial per GCP.Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion.

North Wales, PA30+ days ago

$282,200–$444,200 Per 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.

PA30+ days ago

$282,200–$444,200 Per 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.

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Clinical Research Associate Jobs in Camden, NJ

Associate Scientist Joulé

Associate Director, Forecasting & Performance Analytics, Commercial Operations & Analytics - Remote Agios Pharmaceuticals

Associate Director, Translational Medicine Agios Pharmaceuticals

Associate Director, Scientific Communications & Publications - Remote Agios Pharmaceuticals

Senior Clinical Research Associate ICON Plc

Regional Clinical Research Associate (REMOTE) Teleflex Inc

Senior Clinical Research Associate System One

Senior Clinical Research Associate Johnson & Johnson

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

Clinical Research Associate (CRA) – All levels (I/II/Senior) Theradex Oncology

Senior Clinical Research Associate 6942-ABIOMED Legal Entity

Clinical Research Associate Alexion Pharmaceuticals Inc

Clinical Research Associate ICON Plc

Clinical Research Associate II ICON Plc

Sr. Clinical Research Associate ICON Plc

Senior Clinical Research Associate - East Coast ICON Plc

Lead Clinical Research Associate ICON Plc

Senior Clinical Research Associate-Contractor Systimmune Inc

Senior Clinical Research Associate Systimmune Inc

Sr. Clinical Research Associate Systimmune Inc

Senior Clinical Research Associate-Contractor Systimmune

Sr. Clinical Research Associate Systimmune

Clinical Research Associate I ICON Plc

Clinical Research Associate, Histologist ICON Plc

Clinical Research Associate Impulse Dynamics Germany GmbH

Clinical Research Associate II Systimmune Inc

Clinical Research Associate II Systimmune

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Clinical Research Associate - Oncology - Connecticut ICON Plc

Clinical Research Coordinator-Recruitment Temple University

Clinical Research Coordinator-Katz Temple University

Clinical Research Coordinator Temple University

Clinical Research Integrity Coordinator Temple University Health System

Senior Clinical Research Integrity Coordinator Temple Health

Clinical Research Integrity Coordinator Temple Health

Clinical Research Coordinator B University of Pennsylvania

Clinical Research Coordinator A University of Pennsylvania

Clinical Research Coordinator Senior (HYBRID) - Einstein Thomas Jefferson University

Clinical Research Integrity Coordinator Fox Chase

Senior Clinical Research Integrity Coordinator Fox Chase

Clinical Research Coordinator Nemours

Clinical Research Coordinator Senior Thomas Jefferson University

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

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

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

Clinical Research Assistant Temple University

Clinical Research Coordinator Senior (Neurosurgery) Thomas Jefferson University

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

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

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