623 Results for

Clinical Research Associate Jobs in New Jersey

Jobs

New!

Basking Ridge, NJ3 days ago

$162,400–$243,600 Per Year
Full-time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. This position requires minimal supervision to provide critical study-level support to the CSL/PS/MM/GCL for the successful execution of assigned studies.

Responsibilities.

Basking Ridge, NJ30+ days ago

$153,600–$230,400 Per Year
Full-time

div>

Leadership, Direction, and Strategy:

Establish programming strategy in designing, developing, and maintaining reporting business needs, including programming capabilities assessment, technology and infrastructure requirements of new and/or existing clinical database applications and reporting solutions.
Project Management:
- Drive successful delivery of clinical data management programming objectives by aligning priorities, streamlining workflows, and optimizing resources in collaboration with cross-functional stakeholders.

Basking Ridge, NJ30+ days ago

$100,960–$151,440 Per Year
Full-time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).

Job Description.

Basking Ridge, NJ30+ days ago

$175,440–$263,160 Per Year
Full-time

May participate in meeting or teleconferences with Health Authorities Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.

Qualifications.
Download Our Benefits Summary PDF.

Jersey City, NJ9 days ago

p>The Clinical Development Executive Medical Director is the clinical leader of the specific clinical programs assigned with responsibility for outlining the overall clinical development strategy in line with regulatory requirements and sound scientific rationale, designing the clinical protocols, guiding the Clinical Operations team towards the adequate implementation of such protocols, ensuring adequate medical monitoring activities are implemented for the conduction of clinical studies and analyzing the data from the clinical program. The individual will also be responsible for ensuring adequate implementation of the global safety surveillance and pharmacovigilance for the investigational products, including review and analysis of safety data from clinical trials and other permitted sources (e.g., early access/expanded access programs, if applicable), identification and investigation of safety signals, and management of the benefit-risk profile for assigned compounds.

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.

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.

Cherry Hill, New Jersey7 days ago

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. What You'll Do:

As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies.

New Jersey14 days ago

p>How You Will Add Value:

· Manage and organize all administrative aspects for assigned clinical trials, including creation and maintenance of site personnel contact information, mass mailings, study regulatory documents, electronic or binder preparation for distribution. Impulse Dynamics (USA), Inc. is a fast-growing medical device company that has pioneered a new form of therapy for heart failure called Cardiac Contractility Modulation, or CCM ^TM, which is delivered by the company’s Optimizer^® Smart System.

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.

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.

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, 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.

Parsippany, NJ30+ days ago

$47,400–$169,300 Per Year

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigators Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

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).

Parsippany, Kansas30+ 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. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

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.

Morristown, NJ30+ days ago

Atlantic Health scored four A grades by The Leapfrog Group in its Fall 2025 Hospital Safety Grades, performance measures reflecting errors, accidents, injuries and injections, as well as systems hospitals have in place to prevent harm. Morristown Medical Center is a Magnet Hospital for Excellence in Nursing Service, the highest level of recognition achievable from the American Nurses Credentialing Center for facilities that provide acute care services.

Newark, NJ30+ days ago

Remote

$85–$90 Per Hour

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. The role offers a weekly workload of 40-50 hours, varying by study phase, with opportunities for hybrid work arrangements to support work-life balance.

Parsippany, NJ30+ days ago

p>• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.

Parsippany, NJ30+ days ago

$69,800–$226,800 Per Year

p>Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols, regulations, and sponsor requirements.

Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) according to GCP/ICH and local regulations.

Parsippany, NJ30+ days ago

p>Clinical Research Associate - Sponsor DedicatedParsippany, United States of America | Full time | Field-based | R1541452Job available in additional locations Apply NowShare this jobJob Overview:Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. 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.•

Hackensack, New Jersey10 days ago

Responsibilities:

A day in the life of a Clinical Research Coordinator at Hackensack Meridian Health includes:

Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.
Schedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit.

New Brunswick, NJ30+ days ago

p>To accelerate scientific discovery focused on understanding cancer, innovating cancer treatment, and improving cancer prevention; to provide outstanding, novel, and compassionate patient care; to provide evidence-based and culturally informed education to physicians, nurses, researchers, staff, and the community; and to achieve cancer health equity in our state through outreach to and engagement of our extraordinarily diverse communities. Rutgers Cancer Institute offers world-class quality cancer care providing the most advanced medicines and treatment options for patients in its New Brunswick facility as well as at its network of hospitals across the state through the partnership with the Robert Wood Johnson Barnabas Health System and University Hospital in Newark.

Parsippany, NJ30+ days ago

Deprecated: preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85.

Hackensack, New Jersey30+ days ago

Responsibilities:

Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

New Brunswick, NJ22 days ago

$55–$60 Per Hour

This position assists investigators in preparing and implementing new clinical trials, screens and enrolls study participants, and provides protocol-related clinical management to participants while on study. The position is part of a large clinical operations team with disease-specific groups, contributing to high enrollment needs across multiple sites, including Newark and other locations.

Clifton, NJ30+ days ago

Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

Toms River, NJ30+ days ago

By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.

Hackensack, New Jersey13 days ago

ul>

Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.

The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

New!

Neptune, New Jersey2 days ago

p style="margin:0in"/> Responsibilities:

Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

Union, NJ14 days ago

$22–$23 Per Hour

li>Prepares, completes, organizes and maintains of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documents. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

New Brunswick, NJ22 days ago

$55–$60 Per Hour

The Clinical Research Nurse Coordinator ensures safe, effective, and patient-centered conduct of clinical trials by supporting protocol activation, screening and enrolling participants, and providing protocol-driven clinical management throughout the study. The position bridges direct patient care and research operations, working closely with investigators, multidisciplinary clinical teams, and research administration to maintain regulatory compliance, data integrity, and high-quality oncology nursing care.

Hackensack, NJ30+ days ago

Hackensack Meridian Health nurses care for patients and their families at every stage of life, 24 hours a day, at bedsides in 9 community hospitals, 4 academic medical centers, a behavioral health hospital, 2 children's hospitals, 2 rehabilitation hospitals, medical offices, and care facilities across the state. Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.

NJ30+ days ago

p>A day in the life of a Clinical Research Nurse at Hackensack Meridian Health includes:

Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

Somerset, NJ30+ days ago

$44,900–$61,710 Per Year

p>Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. TMC places a premium on providing customers with world-class products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients.

Nutley, New Jersey30+ days ago

p style="margin:0px">The Center for Discovery and Innovation- CDI was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases. Qualifications:

Education, Knowledge, Skills and Abilities Required:

Bachelor's degree in a science or healthcare related field or 2 years equivalent experience and High School diploma, general equivalency diploma (GED), and/or GED equivalent programs.

Nutley, NJ30+ days ago

p>A day in the life of a Clinical Research Associate at Hackensack Meridian Health includes:

Manages patient recruitment activities and research team training for assigned studies, serves as a liaison with sponsors, other funded sites and coordinates activities across sites nationally and locally.
The Center for Discovery and Innovation- CDI was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases.

NJ30+ 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.

Paramus, NJ30+ days ago

$21.90–$27.37 Per Hour

Short-term and Long-term Disability, Whole Life Insurance, Legal Support, etc.) • 6 Paid Holidays, Paid Time Off (varies), Wellness Time Off, Extended Illness • Retirement Plan • Employee Assistance Program (EAP) • Valley Health LifeStyles Fitness Center Membership Discount • Day Care Discounts for Various Daycare Facilities.

The Clinical Research Support Assistant provides support to the clinical research team by maintaining study inventory, assisting with biospecimen collection and processing, and supporting logistics related to clinical trial conduct.

Secaucus, NJ30+ days ago

Performs study procedures (e.g., obtain ECG recordings, vital signs, safety assessments, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Rahway, NJ12 days ago

$173,200–$272,600 Per Year

Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate 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. The Senior 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.

Rahway, NJ30+ days ago

$282,200–$444,200 Per Year

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. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area.

NJ30+ days ago

$310,900–$489,400 Per 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.

New Brunswick, NJ20 days ago

$54,018–$86,445 Per Year

Saint Peter''s offers a robust benefits program to eligible employees that will support you and your family in working toward achieving and maintaining secure, healthy lives now and into the future. We offer competitive base rates that are determined by many factors, including job-related work experience, internal equity, and industry-specific market data.

Parsippany, California30+ days ago

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).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Stand out to leading employers.

Upload your resume and let employers find you for new Clinical Research Associate job openings. Plus, receive relevant job matches delivered straight to your inbox.

Create A Free Account

Clinical Research Associate Jobs in New Jersey

Associate Director, Clinical Science Daiichi Sankyo, Inc.

Responsibilities.

Associate Director, Clinical Database Applications and Reporting Daiichi Sankyo, Inc.

Sr Clinical Study Assoc CO Daiichi Sankyo, Inc.

Job Description.

Associate Director, Biostatistics (Late Stage) Daiichi Sankyo, Inc.

Qualifications. Download Our Benefits Summary PDF.

Executive Medical Director, Clinical Development - M.D. (Nephrology) Clinical Dynamix, Inc.

Associate Scientist Joulé

Senior Clinical Research Associate System One

Senior Clinical Research Associate 6942-ABIOMED Legal Entity

Senior Clinical Research Associate Johnson & Johnson

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

Clinical Research Associate Zenefitness 85310

Senior Clinical Research Associate-Contractor Systimmune Inc

Sr. Clinical Research Associate Systimmune Inc

Senior Clinical Research Associate Systimmune Inc

Senior Clinical Research Associate-Contractor Systimmune

Sr. Clinical Research Associate Systimmune

Clinical Research Associate, Full Service IQVIA Holdings Inc

Clinical Research Associate Impulse Dynamics Germany GmbH

Clinical Research Associate II Systimmune Inc

Clinical Research Associate - Sponsor Dedicated IQVIA

Clinical Research Associate II Systimmune

Clinical Research Associate, Full Time Days 8a-4p, Atlantic Health, Morristown Medical Center Atlantic Health System Inc

Clinical Research Associate Actalent Inc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Clinical Research Associate, Sponsor Dedicated, Oncology or Immunology IQVIA Holdings Inc

Clinical Research Associate - Sponsor Dedicated IQVIA Holdings Inc

Clinical Research Coordinator Hackensack Meridian Health

Associate Director for Clinical Research (Associate Professor - Professor Rank) Rutgers The State University of New Jersey

Sr. Clinical Research Associate, IQVIA IQVIA Holdings Inc

Clinical Research Nurse - Phase 1 - P/T with Benefits - Days Hackensack Meridian Health

Clinical Research Nurse Coordinator Actalent Inc

Clinical Research Coordinator II Iterative Scopes Inc

Clinical Research Coordinator II - Toms River, NJ Iterative Scopes Inc

Clinical Research Nurse Hackensack Meridian Health

Clinical Research Nurse - JS Hope Tower - F/T Days Hackensack Meridian Health

Clinical Research Coordinator I SGS SA

Clinical Research Nurse Coordinator(peds) Actalent Inc

Clinical Research Nurse - Phase 1 - F/T - Days Hackensack University Medical Center

Clinical Research Nurse Hackensack University Medical Center

Clinical Research Coordinator Terumo Medical Corp

Research Associate - Center for Discovery and Innovation- CDI Hackensack Meridian Health

Research Associate - Center for Discovery and Innovation- CDI Hackensack University Medical Center

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

Clinical Research Support Assistant Full Time Day Clinical Trials The Valley Hospital

Assistant Clinical Research Coordinator/Equipment Supervisor Frontage Clinical Services Inc

Senior Director, Clinical Research, Atherosclerosis Merck & Co Inc

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

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

Clinical Research Coordinator Saint Peter's Healthcare System Inc

Clinical Research Coordinator - Loma Linda, CA IQVIA

Similar Job Searches

Qualifications.
Download Our Benefits Summary PDF.