340 Results for

Clinical Trial Manager Jobs in California

Jobs

New!

Fountain Valley, CA1 day ago

$70,000–$75,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. You will be directly involved in groundbreaking research that has the potential to significantly impact patient care and treatment outcomes in the field of Gynecologic Oncology (GynOnc).

New!

Anaheim, CA1 day ago

$33–$36 Per Hour

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.

New!

Los Angeles, CA1 day ago

$89,000–$100,000 Per Year

This role will oversee the IS PMO's most complex projects, which will likely involve a diverse set of components, including healthcare processes, clinical applications & interfaces, business / administrative applications & interfaces, enabling / supporting technology and infrastructure (e.g., hardware, devices, telecom, storage solutions). Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.

New!

Los Angeles, CA1 day ago

$89,000–$100,000 Per Year

New!

Whittier, CAToday

The clinical trial nurse is required to have comprehensive knowledge in all areas of protocol design, strong clinical assessment and decision-making skills, ability to navigate fast-paced hospital environments, manage multiple studies, excellent communication and patient education abilities, knowledge of federal regulations (FDA, OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). The fully integrated network is comprised of PIH Health Hospital - Whittier, PIH Health Hospital - Downey and PIH Health Good Samaritan Hospital, 27 outpatient medical locations, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, women’s health, urgent care and emergency services.

Work From Home, CA7 days ago

Full-time

Bachelor’s degree and at least 2 years of quota-based sales experience demonstrating a background in cold calling, commissioned, full-cycle sales experience OR at least 5 years of quota-based sales experience demonstrating a background in cold calling, commissioned, full-cycle sales experience. Develop and maintain specific account knowledge within assigned territory such as: key decision makers in each department, department hierarchy, products used and how they are used, company products and competitor’s products, new product process and programs.

New!

San Francisco, CA2 days ago

$2,714.40–$2,714.40

Med/Surg Onc preferred)5 Years RN ExpAbility to float to other UCSF facilitiesPreferredOCN.Telephone triage nursing exp.2 years Outpatient oncology exp.(7/20) Modified 12:00:00 AM Account Manager: Ashley Belarmino Account Manager Email: COVID-19 Vaccine: Required + Booster - Medical/Religious Exemptions only Flu Vaccine: Unknown Job Requirements & Qualifications Previous Charge Experience : Preferred Years of Experience : 5 Patient Ratio Experience : Charting System Experience : Required Charting System Name : Epic Community Hospital Experience : - LTAC Experience : - Trauma Level I Experience : Preferred Trauma Level II Experience : Preferred Travel Experience Required : Yes Certifications : ACLS*, BLS, OCN*, ONS/ONCC*Skills : Administration of chemotherapy, Advanced directives*, Alteration in skin and mucous membranes, Altered mental status, Care coordination, Constipation/diarrhea, Dysphagia, Ear/Nose/Throat Cancers, Edema, Inpatient oncology, Melanoma*, Nausea/vomiting, Neuropathy, Oral Administration of chemotherapy, Outpatient oncology, Patient/Family education and support, Post surgical care, Recognize/ communicate abnormal lab values, Telephone Triage, Tracheostomy care/management, Wound care Unit Details Staffing & Scheduling Scheduling Type : - Patient Ratios Days : - Patient Ratios Nights : - Patient Ratios Weekends : - Float Required : Ability to float to other UCSF facilities Call Required : - Weekend Coverage : - Number of Weekend Shifts Per Contract : - Pre-Approved Time Off : one Orientation Hours : - Facility & Patient Care Details Patient Age Groups : Adults, Geriatrics Daily Census : - Number of Visits Per Day : - Number of Rooms : - Number of Beds : - Additional Unit Information Interdisciplinary Support : - Patient Diagnoses : Head & Neck Medical Oncology: Head and neck cancers including squamous cell carcinoma of the oral cavity, oropharynx, larynx, hypopharynx, nasopharynx, salivary gland tumors, thyroid malignancies, skin cancers of the head and neck, metastatic/recurrent disease, HPV-associated cancers. Head & Neck Surgical Oncology: Head and neck cancers requiring surgical evaluation or treatment including oral cavity tumors, laryngeal cancers, thyroid/parathyroid disease, salivary gland tumors, melanoma and ski Special Procedures/Unit Details : Head & Neck Medical Oncology: Set patients up for chemotherapy, immunotherapy, targeted therapy, symptom management, survivorship care, multidisciplinary coordination with radiation and surgical oncology, clinical trial participation, patient education, nutritional and supportive care management.

Stanford, CA21 days ago

$40–$50 Per Hour
Temporary
Contractor

Manage research project databases, develop flow sheets and other study-related documents, and complete study documents/case report forms. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.

Campbell, CA15 days ago

Full-time

Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer. Contribute operational expertise to the development of study protocols, clinical study documents, and cross-functional clinical initiatives that support innovative neurovascular medical device programs.

South San Francisco, CA30+ days ago

$120,000–$140,000

The CTM will actively participate to help develop and execute the clinical trial strategy in support of the Clinical Development Plan, and to work across departments to ensure that studies are planned and conducted efficiently and with the highest quality. Work with internal team members and CROs in the identification, evaluation and selection of clinical trial investigators and sites, including cooperative groups in multicenter trials as well as in investigator-initiated studies.

Palo Alto, CA21 days ago

$160,000–$170,000

Manages and/or supports vendor management for central laboratory, central IRB, central imaging, patient concierge services, and site payment systems including but not limited to: portal access management for sites and internal teams, report review, sample tracking, metrics review, document reviews and meeting participation . Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.

San Diego, CA30+ days ago

$150,000–$170,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. The Senior Manager, Clinical Trial Transparency and Disclosures (CTTD) is responsible for driving Arrowhead's global transparency strategy, overseeing the planning and execution of clinical trial disclosure activities, and ensuring compliance with international regulations and internal policies.

New!

Foster City, CA3 days ago

$85–$105 Per Hour

The Project Manager will work closely with the Program Lead, Business System Owners, and cross-functional stakeholders to ensure timely, controlled, and inspection-ready transition to Vault Clinical as well as additional projects/workstreams as needed. Project Leadership & DeliveryLead end-to-end planning and execution of Vault Clinical operational setup and existing CTMS decommissioning activities, ensuring alignment with programme timelines and milestones.

San Francisco, CA30+ days ago

Remote

$180,000–$230,000

Experienced Leader: You have 5+ years of experience in health policy, research, or clinical operations, with a demonstrated track record in managing complex initiatives that produce meaningful outcomes. Facilitate the integration of community engagement and ecosystem building methodologies into clinical trial planning and execution, ensuring trials reflect real-world patient diversity.

South San Francisco, California30+ days ago

Employee

South San Francisco, California30+ days ago

Employee

South San Francisco, California30+ days ago

Employee

San Diego, CA30+ days ago

$60,000–$80,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.

South San Francisco, CA27 days ago

$100,000–$120,000

A Clinical Trial Associate (CTA) supports clinical operations by supporting and progressively owning key study execution activities including startup,Trial Master Files (TMF) management, tracking study documents, assisting with site activation, and managing trial reports and supplies. Support Clinical Trial Manager (CTM), Study lead and Study Management Team (SMT) in study start up and executional activities.

Irvine, California22 days ago

Remote

$61,050–$77,000 Per Year

Overview: Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. This role performs invoicing duties and responsibilities throughout the different stages of clinical trials and interacts with healthcare professionals and internal project teams and accounts payable (AP).

Los Angeles, CA30+ days ago

$75,700–$90,000 Per Year
Part-time

The Clinical Research Program Manager works closely with the Director, Principal Investigators (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to manage the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Ability to develop and maintain professional working relationships in complex program/organizational settings involving heterogeneous constituents such as academic and clinical faculty, staff, students, and community partners from diverse backgrounds.

New!

Sacramento, CA3 days ago

$94,848–$142,272 Per Year

Supporting Current Procedural Terminology (CPT)/Healthcare Common Procedure Coding System (HCPCS) billing determinations of clinical trial items and services and applying all applicable local coverage decisions, national and local coverage determinations, and third-party payer rules for clinical trial coverage analyses. Determining and documenting billing support for clinical items by reviewing the protocol, investigator brochures, sponsor budget, sponsor proposed contract, and consent template, the evidence of medical necessity justifications, and appropriate payers of protocol-specific services and federally required research-related claims modifications for service payment by insurance.

Santa Clara, CA30+ days ago

We focus on selecting the right innovations, developing them with precision, and moving them through critical clinical and regulatory milestones so they reach the physicians and patients who need them most. This is a hands-on role responsible for managing and maintaining clinical data systems to ensure accuracy, integrity, and usability of study data.

Orange, California30+ days ago

Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. Responsibilities: Under the general direction of the Assistant Director of Clinical Research Operations of the UCI Center for Clinical Research (CCR), the Clinical Research Manager (CRM) is responsible for all clinical research operational matters in fulfilling the mission of CCR under the University of California Irvine School of Medicine and the overall UC Irvine Health enterprise.

Sunnyvale, CA21 days ago

$72–$74 Per Hour

Experience with development of data management trackers and dashboards (Discrepancy listings, Clean patient tracker, Site trends, study metrics etc.). Provide clinical data management support for study operations and analysis groups and lead clinical data manager.

Irvine, California30+ days ago

Additionally, the incumbent is responsible for leading on-going training and education of CRCs, leading and managing pre-study site selection visits (PSSVs) including liaising with all appropriate ancilliary units (e.g., Investigational Drug Service, Pathology, Radiology, etc.) for the conduct of the trial, managing quality assurance and quality improvement goals and objectives through routine audit reviews of the team’s portfolio. The incumbent is also responsible for maintaining communication with all elements of a multi-level and multi-discipinary research network, including attending Disease Oriented Teams (DOTs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors.

Sacramento, CA30+ days ago

Remote

The Project Manager drives the planning, execution, and delivery of internal initiatives across Study Management functions and reports directly to the Director, Clinical Operations. + Demonstrated end‑to‑end clinical trial management experience across Phase II and Phase III studies, with strong understanding of operational requirements from study start‑up through close‑out.

Irvine, CA30+ days ago

The Case Review Manager leads the patient screening analysis and evaluation of baseline medical history and clinical imaging reports (e.g EDC screening records including clinic notes, lab results, cardiology assessments, CT and/or echocardiogram reports) to confirm protocol compliance and provide patient screening and case review support to clinical trial sites for Clinical Research Trials within THV Clinical Affairs. + Previous related experience working a clinical setting or equivalent work experience based on Edwards criteria Preferred and Experience working in the setting of a clinical trial or equivalent work experience based on Edwards criteria Preferred.

San Diego, CA30+ days ago

$140,000–$170,000 Per Year

Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Minimum of 8 years of relevant experience in clinical operations/clinical quality or quality assurance role/ minimum of 2 years in a managerial or lead role/ minimum of 3 years in TMF experience (preferred).

Irvine, CA30+ days ago

$105,000–$148,000 Per Year

As the Manager, Clinical Contracts and Budgets, you will be responsible for the full clinical contract and budget negotiation lifecycle, partnering closely with clinical study teams, hospitals, vendors, consultants, and cross‑functional groups such as Legal, Finance, and Compliance to develop, negotiate, and lead the execution of a wide range of clinical contracts while applying both legal and clinical expertise. + Draft, negotiate, and execute the full clinical contract lifecycle for a variety of progressively complex contract types at high quality (e.g., Master Clinical Trial Agreements, Statements of Work (including budgets), Non-Disclosure Agreements, and/or Purchase Agreements, utilizing appropriate Edwards templates and systems).

South San Francisco, CA14 days ago

$80–$84.39 Per Hour

Communication and collaboration skills (including consulting skills, interpersonal skills to contribute effectively within- and acrossfunctional team settings, ability to influence others without authority, ability to build strong collaborative relationships with partners). Ensure the timely completion of data management deliverables and partner with Functional Service Providers (FSPs), DM CROs and other vendors, overseeing and providing technical expertise in the delivery of high-quality data.

South San Francisco, CA14 days ago

$41.88–$80.90 Per Hour

The ideal candidate will collaborate cross-functionally to design and implement scalable, high-quality data solutions aligned with F.A.I.R. This role focuses on end-to-end data lifecycle management, supporting exploratory research, clinical development, and evidence generation.

Irvine, California16 days ago

$114,950–$165,000 Per Year

This role works collaboratively with internal stakeholders and external partners, including CROs, vendors, and investigational sites, to ensure the highest quality and integrity of clinical data in support of regulatory submissions and business objectives. Overview: Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease.

New!

Aliso Viejo, CA1 day ago

Facilitate cross-functional Data Management meetings and discussions with Study Managers, Clinical Study Teams, Project Managers, Programming and Regulatory. Assist with writing, reviewing and management of key documents such as Data Management Plan, Project Plan, CRF completion guidelines, edit check specifications, data review guidelines.

Los Angeles, CA30+ days ago

$120,000–$140,000 Per Year

Bachelor's degree in life sciences or technical field; At least 5 years' experience of SAS programming for clinical trials; Working knowledge of SAS, including complex data manipulation, data presentation and output deliver systems; Prior experience implementing edit checks and patient profiles on active clinical trials; and. Develop, and execute edit checks and patient profile software or programs for clinical trials; Develop and execute data listing programs used by data managers, safety surveillance, medical or clinical operations personnel; Collaborate with data management to ensure appropriate data collection and reporting.

Irvine, CA30+ days ago

$157,000–$223,000 Per Year

Develop and lead the execution of Clinical Specialist Device, Imaging, and Field Trainer training programs including lab-based and case-based training with efficient use of resources (Labs, Trainers, Training equipment, etc.). + Partner with Global Training to develop training plans and programs executed through the Edwards Learning Network (ELN) that meet the changing needs and priorities of the business and regions.

Redwood City, CA30+ days ago

Full-time

The ideal candidate will bring strong leadership capabilities, organizational skills, deep expertise in laboratory animal science, and experience supporting the planning and execution of preclinical studies in a fast-paced biotech environment. This individual will serve dual roles, providing operational leadership for our in-house vivarium while also coordinating non-clinical studies conducted with external contract research organizations (CROs).

Martinez, CA30+ days ago

Full-time

Minimum of 7+ years preferred of clinical project management experience in conducting clinical trials in sponsor medical device organization, preferably Class III devices. Process Improvement & TMF RemediationAssess, remediate, and optimize clinical processes and work instructions to align with regulatory requirements, industry best practices, and organizational needs.

Vacaville, CA20 days ago

Full-time

The Clinical Manager works collaboratively with the Clinical Nurse Specialist, Organizational Development, Department Director, related Clinical Managers and Providers to develop and validate the clinical competency of staff, in order to establish a collegial and interdisciplinary patient care environment. The Clinical Manager is a Registered Nurse who has 24-hour responsibility and accountability for the clinical and operational management of Hospital throughput Wound Care Services, including Administrative Coordinators, Discharge Lounge, Transfer Center, Staffing Office and the Center for Wound Care.

New!

Van Nuys, CAToday

$100,000–$135,000

Hands-on EDC experience (Castor, Cloudbyz, REDCap, Medidata, or similar) and comfort working directly with raw data — we care that you get to the bottom of it, not which tool you reach for. Build and refine eCRFs and edit checks that catch bad data at entry (Castor today; we're building our own EDC — you'll help shape the system that makes the truth easy to see).

Los Angeles, CA30+ days ago

$58–$65 Per Hour

The ideal candidate is a seasoned healthcare IT professional who can independently lead workflow design, execute testing strategies, and translate complex clinical requirements into scalable technical solutions that enhance operational efficiency. On behalf of our university client, we are seeking a Senior Clinical Information Systems Analyst to support ambulatory clinical applications within their healthcare IT environment.

Los Angeles, CA30+ days ago

$58–$65 Per Hour

Acting as a key liaison between clinical staff and vendors, the consultant will proactively manage software upgrades, troubleshoot inbound and outbound interfaces, and ensure all systems meet operational, regulatory, and infrastructure requirements. Under the minimal direction of the department leader(s), the Clinical Information Systems Analyst, Senior will be responsible to provide operational support for clinical applications, which include but not limited to Revenue Cycle and Powerchart.

San Diego, CA30+ days ago

$120,000–$140,000 Per Year

Collaborate cross-functionally with Clinical Development, Manufacturing, Regulatory Affairs, and Quality Assurance to plan and execute IMP supply planning including labeling and packaging, utilization forecasting, inventory control, and international shipments and external depot management for Phase 1-4 international clinical studies. Coordinate with Manufacturing Operations, Quality Assurance and Regulatory Affairs to ensure planned IMP release testing/re-testing, stability, expiry dates, labeling and packaging schedules align with program milestones, adjusting as necessary over the course of the program.

New!

Aliso Viejo, CA3 days ago

This role will focus on data cleaning strategies, database management, clinical data review, EDC oversight, and cross-functional collaboration to ensure high-quality, compliant clinical data deliverables. The ideal candidate will have strong project management, analytical, and communication skills with hands-on clinical data management experience within pharmaceutical, biotechnology, medical device, or CRO environments.

New!

National City, CA6 days ago

You will ensure that patients receive quality care by ensuring the store team that provides clinical services follow operational processes and meets their goals daily. Duties & Responsibilities: As a Clinical Services Manager, you will work closely with the Brand Manager to provide supervision and support to the store team to meet clinical goals with guidance from the Clinical Operations Department.

SANTA BARBARA, CA30+ days ago

Full-time

Reviews and evaluates each case by reviewing the services provided by clinicians, instructs and guides clinicians to promote more effective performance and delivery of quality home health services, and is available at all times during operating hours to assist clinicians as appropriate. Leads Team case conference to facilitate coordination of care and assures that patient needs are continually being assessed and is responsible for assuring the development, implementation, and updates of the individualized plan of care.

Fair Oaks, CA29 days ago

$17–$21 Per Hour

San Diego, CA30+ days ago

$131,588.25–$169,704.98 Per Year

Minimum Education: Bachelor's degree Additional Education Requirements Combined experience/education as substitute for minimum education Minimum Experience: 5 years Minimum Skills: Extensive clinical research experience, and experience monitoring clinical research studies. The USC Keck School of Medicine – Alzheimer’s Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert panel of scientific collaborators committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials.

Anaheim, California30+ days ago

$98,454.61–$142,710.62 Per Year

As an associate for a certified Great Place to Work, you will join a collaborative, student-centric culture valuing academic integrity, mutual respect, student learning, service, responsiveness, innovation, diversity, and stewardship. For more than 40 years American Career College has had the privilege of educating students seeking careers in healthcare—guiding them through their transformational journey from student to caregiver.

Anaheim, California30+ days ago

$87,964.06–$127,521.21 Per Year

As a faculty member for a certified Great Place to Work, you will join a collaborative, student-centric culture valuing academic integrity, mutual respect, student learning, service, responsiveness, innovation, diversity, and stewardship. Job Posting Title: Clinical Operations Manager (ACC) Choose To Make A Difference: At American Career College, we share a passion for students and transforming healthcare education!

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Clinical Trial Manager Jobs in California

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Clinical Research Coordinator (Contract) Jobot

Healthcare IT Training Specialist Jobot

Sr Contracts Analyst Jobot

RN Clinical Research, Full time, 8am-4:30pm PIH Health

Sales Rep State and Local Government Medline Industries

Travel Nurse RN - Ambulatory Care - $2,714 per week in San Francisco, CA Prime Staffing

Clinical Research Coordinator(Oncology) Collabera

Clinical Trial Manager Imperative Care

Clinical Trial Manager ALX Oncology Inc.

Senior Clinical Trial Manager - Job ID: 1955 Ascendis Pharma

Senior Manager, Clinical Trial Transparency and Disclosures Arrowhead Pharmaceuticals

Project Manager, Clinical Trial Capabilities, NextGen Clinical Systems support I.T. Solutions, Inc.

GM/CEO, Clinical Trial Abundance Initiative EQL Tech

Strategy Insights & Planning Associate Consultant - Clinical Trials Risk-Based Quality Management (RBQM) ZS

Decision Analytics Associate Consultant - Clinical Trials Risk-Based Quality Management (RBQM) ZS

Business Technology Solutions Associate Consultant - Clinical Trials Risk-Based Quality Management (RBQM) ZS

Clinical Trial Associate Arrowhead Pharmaceuticals

Sr. Clinical Trial Associate ALX Oncology Inc.

Clinical Trial Assistant (Invoicing) - Remote Cordis

Clinical Research Program Manager Charles R. Drew University of Med & Sc

Clinical Trial Coverage Analyst Sutter Health

Clinical Data Manager - T45 Labs T45 Labs

Clinical Research Manager University of California, Irvine

Clinical Data Manager eTeam Inc.

Clinical Research Manager - Hybrid University of California, Irvine

Clinical Project Manager - East Coast US - FSP Parexel

Manager, Clinical Case Review Edwards Lifesciences

Senior Manager, Clinical Standards & Processes Arrowhead Pharmaceuticals

Manager, Clinical Contracts and Budgets Edwards Lifesciences

Clinical Data Manager II Integrated Resources, Inc

Clinical Data Manager II Tailored Management

Clinical Study Manager Cordis

Clinical Data Manager Trident Consulting

Manager, Clinical Programming Arrowhead Pharmaceuticals

Clinical Education Manager, Global Training and Expansion Edwards Lifesciences

Senior Manager, Non-Clinical Studies & Vivarium Operations ImmunEdge, Inc

Clinical Operations Manager ExThera Medical

Clinical Manager, Wound Care, Clinical Support Services and Transfer Center Northbay Healthcare

Clinical Data Manager - Data Integrity & Investigation RDI

Project Manager Clinical Tucker Parker Smith Group (TPS Group)

Project Manager Clinical Artech LLC

Manager, Clinical Supply Management Arrowhead Pharmaceuticals

Clinical Data Manager II Trident Consulting

Clinical Services Manager Physicians Eye Care Group

Clinical Manager - Home Health VNA Health

Clinical Services Manager Stanton Optical

Clinical Monitoring Line Manager University of Southern California

Clinical Manager, Radiography American Career College

Clinical Operations Manager (ACC) American Career College

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