Clinical Risk Management Specialist - Trials & Quality
Johnson & Johnson Innovative Medicine
Johnson & Johnson Innovative Medicine is seeking a Specialist, Clinical Risk Management to coordinate risk identification, assessment, and mitigation across trials. You will execute data-driven oversight to maintain trial data integrity, patient safety, and compliance with regulatory requirements. The role requires 4+ years in healthcare or pharma, CSP/ICH experience, strong communication, and a collaborative, global mindset. Travel up to 10% domestically/internationally may be required. #J-18808-Ljbffr Johnson & Johnson Innovative Medicine
- ...labor as a variable cost.Job DescriptionThe Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in... ...rework operations.• Constant interaction with quality (SQO), making sure that all activities...QualityWork at officeLocal areaImmediate start
- Johnson & Johnson in New Jersey is seeking a Specialist, Clinical Risk Management to coordinate identification, assessment, and mitigation of quality risks across clinical trials. You will work with trial teams to deliver risk-based oversight, ensure compliance with regulatory...Quality
- ...implementation and conduct of studies (clinical trials, observational studies, compassionate use and registries) including data management activities in compliance with GCP’s, SOPs... ...to guarantee release of homogeneous high quality data, in close collaboration with other...QualityImmediate startFlexible hours
$109.8k - $164.7k
...potential?Reporting StructureReports To: Director, Clinical Operations NADirect Reports: NoneAreas Managed: Clinical trials in North AmericaOverviewThe Clinical Trial... ...subject recruitment, protocol adherence, and data quality. The CTLM represents RRD in site relations,...QualityTemporary workInterim roleWork at officeLocal areaRemote workNight shiftWeekend work3 days per week- Precision for Medicine is seeking a Manager Clinical Trial Management in New Jersey to lead and grow a team of Clinical Trial Managers and Principal CTMs. The role focuses on quality, SOP compliance and implementing department initiatives to boost productivity. Responsibilities...Quality
- Precision Medicine Group is seeking a clinical trial lead to oversee the operational aspects of clinical studies,... ..., ICH-GCP, and regulatory requirements. You will manage feasibility, site start-up, enrollment, and quality deliverables while coordinating with PM, CRAs, and...Quality
$75k - $125k
...services firm that helps clinical research sites, sponsors, and CROs improve trial activation, operational... ...address billing compliance risks, ensuring adherence to... ...client engagements, managing competing priorities while maintaining high-quality deliverables. Required...QualityFull timeRemote workFlexible hours$75k - $125k
...Vitalief Vitalief is a clinical research consulting... ...professional with deep clinical trial budgeting expertise to... ...billing compliance risks while ensuring... ...engagements, effectively managing competing priorities while delivering high-quality results. Qualifications...QualityFull timeTemporary workRemote workFlexible hours- ...training. Position Description: Supports timely delivery of clinical supplies through effective management of assigned projects. Manages multiple projects and... ...teams in various areas. Liaises with responsible Trial Supplies Manager on aspects of clinical supplies packaging...QualityFull timeWork from home
- ...Clinical Data Analyst A Few Words About Us Integrated Resources... ...on delivering only the best quality talent, the first time and every... ...client Job Description Manage IVRS upload jobs Upload... ...familiar with the Clinical Trials Management process Qualifications...Quality
$133.9k - $200.9k
...Position Summary The Manager Clinical Trial Management (MCTM) offers an additional development path... ...departmental initiatives to strengthen the quality and productivity of Clinical Trial... ...guidance (including scope definition, risk identification, escalation and mitigation...QualityWork experience placementWork at officeLocal areaNight shift- Precision Medicine Group seeks a Senior Project Manager to lead clinical study activities, ensuring quality, scope, cost, and time objectives are met. You will act as the main client contact and oversee vendors to maintain timelines and budget. Responsibilities include...Quality
$32 - $38 per hour
...Description Job Description Job Title: Clinical Trial Specialist Job Description This role offers... ...practice by coordinating and managing cancer clinical trials, ensuring that... ...functions in research administration, quality assurance, informatics, education, and...QualityFull timeContract workTemporary workWork at office- A leading healthcare organization based in New Jersey is looking for a Senior Project Manager. This role involves planning and directing clinical study projects, ensuring quality and timely delivery while managing budgets. The ideal candidate will have over 7 years of...Quality
- ...Lead Clinical Research Associate Integrated Resources, Inc is a... ...on delivering only the best quality talent, the first time and every... ...• Development, execution, management and compliance assurance of the... ...collection and filing into the Trial Master File Qualifications...QualityWork at office
- ...Medical Director of Neurology, Clinical Development holds the... ...and interpretation of clinical trial data, authoring clinical study... ...protocols and delivering high-quality clinical programs, from first... ...charters, or other specific management plans and manuals in a cross-...Quality
- Role Overview The QA Shop Floor Specialist is an exempt level position responsible for the floor quality oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. This role is responsible...QualityLocal areaImmediate startWeekend work
- ...Biotech in Raritan, NJ is seeking a QC Analyst I (IPL) to perform QC testing related to manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. The role requires a Bachelor's degree in science or engineering, at...QualityWeekend workAfternoon shift
$110.7k - $200.9k
Position Summary Serves as the clinical trial lead responsible for the... ...monthly invoicing and variance management of clinical budget Develop... ...process Identify potential risks to the enrollment targets... ...timelines are met and assuring quality deliverables Generate and...QualityContract workWork experience placementWork at officeFlexible hoursNight shift$96.27k - $126.35k
...Overview The QA Shop Floor Specialist is an exempt level... ...for floor quality oversight of the production... ...autologous CAR‑T products for clinical trials and commercial... ...processes as assigned by management and continue to... ...compliance and minimize risk. Ability to...QualityPermanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaImmediate startFlexible hoursWeekend workDay shift- ...Description• This role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science &... ...prior patients' data review as needed• Ensure high quality execution from a medical perspective with support of all functions...QualityWork at officeLocal area
$128.8k - $171.7k
...Description and Requirements The Team You Will JoinJoin our Global Risk Management Group, where you’ll play a key role in safeguarding the... ...with use case owners to improve submission quality, ensuring completeness and alignment with governance standardsCoordinate...QualityFull timeTemporary workWork at officeLocal areaRelocation package3 days per week- ...Raritan, NJ, responsible for QC testing of CAR‑T products for clinical trials and commercial operations. The role demands compliance with... ...a relevant field and have at least one year of experience in Quality Control, preferably within the biological or pharmaceutical sectors...QualityNight shift
$170k - $190k
The Senior Clinical Trial Drug Supply Manager is a critical position within the clinical development organization... ..., supply coordination, internal quality, packaging, distribution and expiry date... ...to detail, particularly in high-risk, patient-critical supply environmentsEffective...QualityTemporary workWork at officeFlexible hours$285k - $315k
...Title Senior Director, Clinical Development Requisition... ...responsible for oversight and management of the clinical development execution... ...Ensure CD contributions to trial-related documents such as the... ...purpose drives us as we pair quality therapeutics with human...QualityWork at officeFlexible hours$75.97k - $99.71k
...Role Overview Legend Biotech is seeking a QA Shop Floor Specialist II/III as part of the Quality Operations team based in Raritan, New Jersey . The... ...of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom...QualityWork experience placementImmediate startWorldwideFlexible hoursWeekend work$83.71k - $109.87k
...for multiple myeloma. Sr. QC Analyst - Quality team, Raritan, NJ Shift: 3rd shift Wed‑... ...manufacturing of cell therapy products for clinical trials and commercial operations in a... ...outcomes in decisions. Employs good project management principles to align time, resources and...QualityPermanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaWorldwideFlexible hoursShift workNight shiftAfternoon shift- ...Biotech is seeking participants for Legend's Manufacturing/Quality Management, Leadership Development Program as part of the Technical... ...functions. Legend's U.S. manufacturing network supports clinical trials and commercial CARVYKTI® available at more than 140 treatment...QualityPermanent employmentFull timeFor contractorsLocal areaWorldwide
$226k - $391k
...Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub... ...plans (including life-cycle management, geographic expansion, and post... ...commitments), protocol development, quality execution of clinical studies... ...for the design of clinical trials and for the content of...QualityFull timeTemporary workImmediate start$164k - $282.9k
...merit.Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:... ...Clinical Leads, to design, plan, and manage complex clinical trials, ensuring compliance with departmental... ...execution of clinical studies.• Maintain the quality and integrity of clinical data...QualityFull timeWork at officeLocal areaImmediate startRemote work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Risk Management Specialist - Trials & Quality. Be the first to apply!


