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Remote Jobs in Riverside, ND

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Industry Liaison (Oncology Studies) System One

Philadelphia, PA

$160,000 / year
Quick Apply

In this direct-hire role, you’ll serve as a key liaison between the organization and pharmaceutical industry partners, supporting oncology clinical trials from study development through closeout while coordinating cross-functional stakeholders (clinical operations, protocol development, contracts/budgets, data teams, and vendors). Coordinate pharmaceutical industry related activities within the Operations office, including collaborating with grants and contracts team, clinical operations team, protocol development team, lab science team, data management, and statistical teams.

4 days ago

Senior Project Manager System One

Philadelphia, PA

$160,000 / year
Quick Apply

Supervise development of cross-functional project teams including Medical, Data Management, Regulatory, Monitoring, and Clinical Supplies departments. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.

4 days ago

Revenue Integrity Analyst, Epic Revenue Cycle Analyst, Mt. Laurel VIRTUA

Mount Laurel, NJ

Incumbent must develop close working relationships with management and staff in Revenue Integrity, Finance, Information Technology and Revenue and Clinical Operations allowing them to perform deep-dive analysis and reviews assisting with the identification of trends, solutions and potential corrective action steps. Work with Revenue Integrity Team, Clinical Operations and Patient Financial Services staff to implement corrective actions to ensure compliant charges, prevent future rejections/denials and accurate and reimbursement.

1 day ago

Clinical Study Manager, Global Clinical Operations - 30014765 Daiichi Sankyo Co Ltd

Basking Ridge, NJ

$133,600–$200,400 / year

CRO Oversight: Responsible for the oversight, performance, and management of CRO(s) and 3rd party vendors (sub-contracted by CRO) to ensure compliance with Daiichi Sankyo's quality measures and adherence to scope of work within timelines and budget at a task level. Clinical Operations Study Management(Global) has primary accountability for operational execution and delivery of assigned clinical trials, including study level time, cost and quality deliverables.

30+ days ago

Senior Manager, Clinical Operations PTC Therapeutics

Warren, NJ

$136,600–$171,900 / year

The Senior Manager collaborates cross-functionally with internal and external stakeholders and external service providers to ensure the successful delivery of clinical trials with respect to quality, timelines, and budget. Job Description Summary: The Senior Manager, Clinical Operations is responsible for the operational planning, execution, and oversight of clinical trials supporting the company's clinical development programs.

19 days ago

Provider Clinical Operations Consultant, Manager PricewaterhouseCoopers LLP

Philadelphia, PA

$99,000–$232,000 / year

Preference for at least one of the following fields of study: Accounting, Actuarial Science, Analytics/Data Science, Business Administration/Management, Computer Science/Information Systems, Economics, Engineering, Finance, Government/Public Policy, Health Administration/Public Health, Mathematics/Statistics, Operations/Supply Chain, Organizational Management/Behavior, Risk Management/Insurance. As a Provider Clinical Operations Consultant, Manager you will lead client service workstreams focused on provider clinical operations, bringing together operations consulting methods, health services knowledge, and process improvement skills to support clinical modernization efforts within our Operations Consulting practice.

6 days ago

Senior Scientist, Study Manager - Atherosclerosis and Metabolism Clinical Operations Merck & Co Inc

Rahway, NJ

$117,000–$184,200 / year

May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities). Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.

5 days ago

Senior Scientist, Regulatory & Clinical Operations hims & hers

South Plainfield, NJ

You Have: PhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master's degree with 7+ years; OR Bachelor's degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting. The ideal candidate is comfortable operating at the intersection of bench science and clinical study execution, translates regulatory rigor into practical day-to-day decisions, and thrives working independently in a fast-moving environment.

30+ days ago

Clinical Quality Operations Manager- Remote Merck & Co Inc

Rahway, NJ

Remote

$142,400–$224,100 / year

Required Skills: CAPA Management, Clinical Quality Management, Communication, Cross-Functional Teamwork, Data Analysis, Good Clinical Practice (GCP), Process Improvements, Project Management, Regulatory Compliance, Regulatory Inspections, Risk Management, Root Cause Identification, Strategic Thinking, Taking Initiative. The CQOM will provide clinical quality operations support to Trial Teams (TTs) to proactively embed quality into sponsored trials, ensure robust supplier oversight, and address critical quality issues as needed.

3 days ago

Senior Director, Clinical Operations Program Lead Kardigan

Princeton, New Jersey

$247,000–$322,000 / year

This position will be responsible for leading all of the activities associated with the clinical studies for the asset across all phases, including overseeing the internal operations team, CROs and vendors and working cross-functionally on the operational strategy and related initiatives. This position will work collaboratively across the department, the entire Kardigan portfolio and cross-functional core/project teams with the overall goal of developing new and innovative treatments for cardiovascular diseases with unmet need.

9 days ago

Associate Director, Clinical Operations Summit Therapeutics Inc

Princeton, NJ

$174,000–$205,000 / year

HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. Drafts, reviews and approves internal and external study-related plans, processes, and documents including Informed Consent Forms, Investigator Agreements (CTA), CRFs, CRF Guidelines, statistical/pharmacokinetic analysis plans, monitoring plans, data management plans, and safety monitoring activities.

30+ days ago

Associate Director, Clinical Operations PTC Therapeutics Inc

Warren, NJ

$170,200–$214,200 / year

Primary duties/responsibilities: Performs as an integrated member of the clinical team to lead, direct and contribute to, the planning, execution, and reporting of clinical trials, including estimation of clinical project timelines, protocol writing, Case Report Form (CRF) design, site selection, study drug forecasting, site and Clinical Research Organization (CRO) management, data review, and study reporting; recommends monitoring, safety, eligibility, enrollment, and data consistency strategies. Manages clinical study timelines using the appropriate project management tools; develops budgets and manages expenditures for clinical trial program, including those for investigational sites and vendors; presents project progress reports through accurate, succinct summaries of clinical study work at internal team meetings and investigator meetings.

30+ days ago

Clinical Research Operations Manager - Oncology Vitalief

Somerset, NJ

$115,000–$150,000 / year

By combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

30+ days ago

cGMP Operations and Clinical Specialist University of Pennsylvania

Philadelphia, PA

$62,000–$70,000 / year

For the HIC, the Specialist will coordinate administrative and operational activities related to research donors, including scheduling and coordinating donor activities, processing and tracking payments, maintaining appropriate documentation and records, coordinating communications, and serving as a liaison among HIC, CVPF, CCI, and other stakeholders. The role will also support communication and coordination among investigators, research staff, administrative teams, institutional offices, and other stakeholders to ensure grant activities remain organized, timelines are maintained, reporting requirements are met, and administrative tasks are completed accurately and on time.

30+ days ago

Senior Scientist, Regulatory & Clinical Operations Hims & Hers

South Plainfield, New Jersey

PhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master’s degree with 7+ years; OR Bachelor’s degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting. The ideal candidate is comfortable operating at the intersection of bench science and clinical study execution, translates regulatory rigor into practical day-to-day decisions, and thrives working independently in a fast-moving environment.

30+ days ago

Associate Director Clinical Operations ACADIA PHARMACEUTICALS INC

Princeton, NJ

$147,900–$184,900 / year

Prepares/oversees the preparation of all applicable documents required for the conduct of the study (Project Plan, Risk Management Plan, Monitoring Plan, Trial Master File (TMF)) etc.* Manages and reviews the work of Contract Research Organization (CRO) to ensure that tasks are performed to scope and budget.* We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs.

30+ days ago

Director, Clinical Research Operations Transformation Vitalief

Orange, NJ

As the primary subject matter expert (SME), this leader will collaborate closely with the Vitalief delivery team to design and implement enterprise-level operational initiatives, with a strong emphasis on Non-Oncology programs and enhancing cross-system communication and coordination. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

30+ days ago

Senior Director, Clinical Research Operations Vitalief

Orange, NJ

30+ days ago

Director, Clinical Research Operations Service Line Activation Vitalief

New Brunswick, NJ

Full time

Cardiovascular, pulmonary, or cardiopulmonary clinical research experience is required: a track record running industry trials in cardiology and vascular medicine (drug, device, structural heart, heart failure, or cardiometabolic trials), in pulmonary or critical care medicine (Phase 2 and 3 drug studies, inhaled and biologic therapies, device and interventional pulmonology, or ICU trials), or across both. Manage Portfolio & Working Group: Lead the service line expert working group, establish regular cadence, identify and resolve cross-study bottlenecks, and steward priority studies from startup through enrollment, escalating enterprise-level issues as needed.

30+ days ago

Vice President of Clinical Operations (RN) Vitality Hospice

Toms River, NJ

We're seeking an experienced Vice President of Clinical Operations (RN) to provide strategic leadership, oversee clinical operations, ensure regulatory compliance, and inspire our interdisciplinary team to deliver exceptional hospice care. At Vitality Hospice & Palliative Care , we're committed to providing compassionate, patient-centered end-of-life care while creating a supportive workplace where our employees feel valued, respected, and empowered.

3 days ago

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Remote Jobs in Riverside, ND

Industry Liaison (Oncology Studies) System One

Senior Project Manager System One

Revenue Integrity Analyst, Epic Revenue Cycle Analyst, Mt. Laurel VIRTUA

Clinical Study Manager, Global Clinical Operations - 30014765 Daiichi Sankyo Co Ltd

Senior Manager, Clinical Operations PTC Therapeutics

Provider Clinical Operations Consultant, Manager PricewaterhouseCoopers LLP

Senior Scientist, Study Manager - Atherosclerosis and Metabolism Clinical Operations Merck & Co Inc

Senior Scientist, Regulatory & Clinical Operations hims & hers

Clinical Quality Operations Manager- Remote Merck & Co Inc

Senior Director, Clinical Operations Program Lead Kardigan

Associate Director, Clinical Operations Summit Therapeutics Inc

Associate Director, Clinical Operations PTC Therapeutics Inc

Clinical Research Operations Manager - Oncology Vitalief

cGMP Operations and Clinical Specialist University of Pennsylvania

Senior Scientist, Regulatory & Clinical Operations Hims & Hers

Associate Director Clinical Operations ACADIA PHARMACEUTICALS INC

Director, Clinical Research Operations Transformation Vitalief

Senior Director, Clinical Research Operations Vitalief

Director, Clinical Research Operations Service Line Activation Vitalief

Vice President of Clinical Operations (RN) Vitality Hospice

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