684 Results for

Clinical Research Associate Jobs in Pennsylvania

Jobs

Bethlehem, PA

Full time

Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.

6 days ago

Allentown, PA

Full time

30+ days ago

Carnegie, PA

A top-ranked research university is currently searching for a Clinical Research Coordinator III for one of its growing departments to be for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process.

Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes.

8 days ago

Philadelphia, PA

Remote

$153,541–$230,312 / 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.

6 days ago

Philadelphia, PA

$153,541–$230,312 / 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.

6 days ago

Philadelphia, PA

Remote

$153,000–$230,000 / 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.

6 days ago

Pittsburgh, PA

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Ability to establish and maintain positive, caring relationships with executives, managers, physicians, non-physician providers, ancillary and support staff, other departments, and patients/families.

Demonstrates a basic knowledge of research, how it affects practice and who/what resources are available to assist with evidence-based practice by asking questions, demonstrating interest, participating in journal clubs.

2 days ago

Mars, PA

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Ability to establish and maintain positive, caring relationships with executives, managers, physicians, non-physician providers, ancillary and support staff, other departments, and patients/families.

The successful completion of an approved Nurse Practitioner or a graduate of a physician assistant program accredited by the Accreditation Review Commission on Education for the physician assistant (ARC-PA) program is required .

16 days ago

Sewickley, PA

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Ability to establish and maintain positive, caring relationships with executives, managers, physicians, non-physician providers, ancillary and support staff, other departments, and patients/families. The CNM, Staff establishes and maintains collaborative relationships with physicians, other health care providers, patients and their families, to achieve desired patient outcomes throughout the continuum of care.

Today

Allentown, PA

Full time

Prepare, maintain, and file all essential regulatory documentation required by sponsor or CRO (1572s, Financial Disclosure Forms, Delegation Logs, CVs and Medical Licenses, FCOI forms, SAEs and UAPs, training logs, etc.) within the study and regulatory binders. Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care.

14 days ago

Blue Bell, PA

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.

30+ 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

Pittsburgh, PA

The Associates responsibilities will entail, but not be limited to, assisting with the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials. Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.

30+ days ago

Remote

$97,000–$193,000 / 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.

13 days ago

Pittsburgh, PA

The Clinical Research Associate will be working in the ICU setting, coordinating interventional clinical trials alongside the APP, bedside nurses, and physicians, and drawing/processing blood samples from patients, overseeing data management of large-scale trials. The Multidisciplinary Acute Care Research Organization (MACRO provides clinical trial services to principal investigators seeking to maximize the productivity and efficiency of acute care research, from the pre-hospital setting to the ICU and inpatient wards.

29 days ago

Pittsburgh, PA

Full time

Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience. The Associate's responsibilities will entail, but not be limited to, assisting with the management and inventory of clinical supplies, ensuring proper materials are available at clinical sites in a timely manner, and working with the Clinical Operations team to support multiple Clinical Trials.

30+ days ago

Blue Bell, PA

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

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

$110,520–$138,150 / year

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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

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.

2 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, 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.

20 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.

5 days ago

Hershey, PA

Either Associates Degree in a science or healthcare related field which includes job related coursework required or three (3) years experience in a healthcare or research setting required or Bachelors degree in a science or healthcare related field. Penn State Health offers an exceptional benefits package, including: • Medical, dental, and vision with no waiting period • Total Rewards Program that highlights a few of the many additional offerings below • Be Well: with Employee Wellness Programs and Fitness Discounts • University Fitness Center • Peloton.

30+ days ago

Pittsburgh, PA

Remote

The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that areallocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolutediscretion, consistent with applicable law. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this roleat the time of this posting based on the job grade for this position.

16 days ago

Hershey, PA

Be Balanced: with Generous Paid Time Off, Personal Time, and Paid Parental Leave • Be Secured: with Retirement, Extended Illness Bank, Life Insurance, and Identity Theft Protection • Be Rewarded: with Competitive Pay, Tuition Reimbursement, and PAWS UP employee recognition program • Be Supported: with the HR Solution Center, Learning and Organizational Development, and Virtual Benefits Orientation • Employee Exclusive Concierge Service for scheduling. Associates Degree plus three years of experience in a healthcare or research setting required or five years of experience in a healthcare or research setting required or Bachelors degree plus one year or experience.

30+ 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

Wilkes-Barre, PA

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, 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

Pittsburgh, PA

In connection with this, all employees must comply with both the Health Insurance Portability Accountability Act of 1996 (HIPAA) as described in the Notice of Privacy Practices and Privacy Policies and Procedures as well as all data security guidelines established within the Company's Handbook of Privacy Policies and Practices and Information Security Policy. Certified Clinical Research Coordinator (CCRC), ACRP Certified Professional (ACRP-CP) or The Society of Clinical Research Associates (SOCRA), Certified Clinical Research Professionals (CCRP).

30+ days ago

Pittsburgh, PA

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

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.

6 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''.

6 days ago

Philadelphia, PA

$52,500–$53,418 / 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.

30+ days ago

Allentown, PA

Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. EDUCATION: Bachelor's degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.

30+ days ago

Bethlehem, PA

EDUCATION:

Bachelor's degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.

6 days ago

Philadelphia, Pennsylvania

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.

9 days ago

Philadelphia, PA

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.

27 days ago

Hershey, PA

p>SUMMARY OF POSITION:

Responsible for the facilitation, coordination and implementation of clinical research protocols under physician investigator guidance and delegation, including liaison with faculty and external sponsors/agencies, patient management and education, budget review and quality management.

Penn State Health offers an exceptional benefits package including medical, dental and vision with no waiting period as well as a Total Rewards Program that highlights a few of the many additional offerings below:

Be Well with Employee Wellness Programs, and Fitness Discounts (University Fitness Center, Peloton).

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.

6 days ago

Philadelphia, PA

30+ days ago

Lancaster, PA

Qualified individuals must have the ability with or without reasonable accommodation to perform the following duties: Plans and coordinates assigned research studies, serves as principle liaison for the project, interfaces with research subjects and collects research data, oversees administrative support, develops appropriate tools needed to conduct the research, and maintains record keeping systems and procedures. Functions as a resource for physicians, other health care providers, and ancillary support staff regarding care of the research participant as it relates to any given clinical research protocol; conducts staff in-services as appropriate.

17 days ago

Lancaster, PA

p>Loading job Back to Search Results Previous Opportunity Next Opportunity Current UPHS employees must apply HERE Registered Nurse RN Clinical Research Coordinator (Full Time/Days) Job ID: 306018 Category: Nursing Work Type: FT Location: Lancaster, PA, United States Share: share to e-mail Apply Now Save Job Saved Description Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Qualified individuals must have the ability with or without reasonable accommodation to perform the following duties: Plans and coordinates assigned research studies, serves as principle liaison for the project, interfaces with research subjects and collects research data, oversees administrative support, develops appropriate tools needed to conduct the research, and maintains record keeping systems and procedures.

30+ days ago

Philadelphia, PA
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.
30+ 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.
22 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.
30+ days ago

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Clinical Research Associate Jobs in Pennsylvania

Clinical Research Coordinator I (PA/NJ residents only) St. Luke's Health Network, Inc.

Clinical Research Coordinator I- Precision Medicine St. Luke's Health Network, Inc.

Clinical Research Coordinator III 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

PA or CRNP, PrimeCare Medical Associates UPMC - University of Pittsburgh Medical Center

CRNP or PA, Staff or Senior (Womancare Associates) UPMC - University of Pittsburgh Medical Center

Midwife - UPMC Womancare Associates UPMC - University of Pittsburgh Medical Center

Regulatory Coordinator I St. Luke's Health Network, Inc.

Senior Clinical Research Associate ICON Plc

Regional Clinical Research Associate (REMOTE) Teleflex Inc

Clinical Trial Associate/Clinical Research Coordinator Krystal Biotech Inc

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

Casual Clinical Research Associate University of Pittsburgh Medical Center

Clinical Trial Associate/Clinical Research Coordinator Krystal Biotech

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

Clinical Research Associate I ICON Plc

Clinical Research Associate, Histologist ICON Plc

Associate Clinical Research I - Clin HV Cardio Research Penn State Milton S Hershey Medical Center

Clinical Research Associate II - Oncology Remote US - Multiple Openings AbbVie Inc

Associate Clinical Research II - Heart & Vascular Admin Penn State Milton S Hershey Medical Center

Clinical Research Associate - Oncology - Connecticut ICON Plc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Clinical Research Coordinator-Recruitment Temple University

Clinical Research Coordinator Temple University

Clinical Research Coordinator-Katz Temple University

Clinical Research Coordinator / Part-time Highmark Inc

Clinical Research Coordinator - Full Time - Day Shift - AGH Highmark Inc

Senior Clinical Research Integrity Coordinator Temple Health

Clinical Research Integrity Coordinator Temple Health

Clinical Research Integrity Coordinator Temple University Health System

Clinical Research Coordinator B University of Pennsylvania

Clinical Research Coordinator I - Precision Medicine St. Luke's University Health Network

Clinical Research Coordinator I (PA/NJ residents only) St. Luke's University Health Network

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

Clinical Research Coordinator A University of Pennsylvania

Coordinator Clinical Research II - Clin HV Cardio Research Penn State Milton S Hershey Medical Center

Clinical Research Integrity Coordinator Fox Chase

Senior Clinical Research Integrity Coordinator Fox Chase

Registered Nurse Clinical Research Coordinator (Full Time/Days) Penn Medicine

Registered Nurse RN Clinical Research Coordinator (Full Time/Days) Penn Medicine

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

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