Current jobs related to Clinical Trial Manager/site Monitoring - Ridgefield - Adientone

  • Clinical Trials Operations Manager

    4 weeks ago

    Ridgefield, Connecticut, United States Maxis Clinical Sciences Full time

    Job OverviewPosition: Clinical Trials Operations ManagerResponsibilities:As the Clinical Trials Operations Manager, you will be responsible for overseeing the operational aspects of clinical trials at a local level. Your leadership will ensure that recruitment targets, timelines, budgets, and quality standards are met.You will lead the local trial team to...

  • Clinical Trial Specialist

    4 months ago

    Ridgefield, United States McInnis Inc. Full time

    Job DescriptionJob DescriptionClinical Trial Operations (CTO)The CTO will work remotely as a member of the Clinical Trial Team in the Study Management and Conduct Group supporting the Clinical Trial Leader (CTL), Clinical Trial Manager (CTM), and Feasibility Manager (FM). The CTO is responsible for end-to-end site management activities.In addition, may be...

  • Clinical Trials Operations Manager

    1 month ago

    Ridgefield, Connecticut, United States Compunnel Inc. Full time

    Job Title: Clinical Trials Operations ManagerLocation: RemoteJob Overview:As the Clinical Trials Operations Manager, you will be responsible for overseeing the operational aspects of clinical trials. Your role is crucial in ensuring that recruitment goals, timelines, budgets, and quality standards are met throughout the trial process.Key...

  • Manager of Clinical Research Trials

    1 month ago

    Ridgefield, Connecticut, United States SPECTRAFORCE Full time

    Position: Clinical Trial Manager (REMOTE)Contract Duration: 12 MonthsCompensation: Starting at $65/hr on W2 (Negotiable)Key Responsibilities:As the Clinical Trial Manager (CTM), you will be responsible for overseeing the operational aspects of the local segment of a clinical trial.Your oversight will ensure that recruitment targets, timelines, budgetary...

  • Clinical Research Operations Manager

    4 weeks ago

    Ridgefield, Connecticut, United States Maxis Clinical Sciences Full time

    Job OverviewPosition Title: Clinical Research Operations ManagerResponsibilities:As the Clinical Research Operations Manager, you will be responsible for overseeing the operational aspects of clinical trials at a local level. Your leadership will ensure that recruitment goals, timelines, budgets, and quality standards are met consistently.In this role, you...

  • Clinical Trials Operations Lead

    4 weeks ago

    Ridgefield, Connecticut, United States Nexpro Technologies Inc Full time

    Job OverviewPosition: Clinical Trials Operations LeadResponsibilities: As the Clinical Trials Operations Lead, you will be responsible for overseeing the operational aspects of clinical trials at a local level. Your leadership will ensure that recruitment goals, timelines, budgets, and quality standards are met consistently.Team Leadership: You will guide...

  • Clinical Research Operations Manager

    1 month ago

    Ridgefield, Connecticut, United States SPECTRAFORCE Full time

    Job Title: Clinical Research Operations Manager (REMOTE)Duration: 12 MonthsPay Rate starts from $65/hr on W2 (Negotiable)Key Responsibilities:As the Clinical Research Operations Manager, you will be responsible for overseeing the operational aspects of clinical trials.Your role will ensure that recruitment goals, timelines, budgets, and quality standards are...

  • Clinical Research Associate

    4 months ago

    Ridgefield, United States McInnis Inc. Full time

    Job DescriptionJob DescriptionThe Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned...

  • Clinical Trials and Pharmacovigilance Expert

    3 weeks ago

    Ridgefield, Connecticut, United States McInnis Inc. Full time

    Job DescriptionJob Title: Pharmacovigilance and SafetyCompany: McInnis Inc.Job Type: Full-timeLocation: RemoteJob Description:We are seeking a highly skilled Pharmacovigilance and Safety professional to join our team. As a key member of our Pharmacovigilance and Risk Management department, you will be responsible for assessing individual clinical trials and...

  • Clinical Data Entry Coordinator

    2 days ago

    Ridgefield, Connecticut, United States McInnis Inc. Full time

    Job SummaryWe are seeking a highly skilled Clinical Data Entry Coordinator to join our team at McInnis Inc. The successful candidate will be responsible for accurately entering data into various applications, maintaining investigator and site data, and resolving quality issues with clinical operations personnel.Key ResponsibilitiesEnter accurate information...

  • Clinical Trial and Pharmacovigilance Expert

    4 weeks ago

    Ridgefield, Connecticut, United States McInnis Inc. Full time

    Job DescriptionJob Title: Pharmacovigilance and Safety SpecialistCompany: McInnis Inc.Job Type: Full-time/Part-timeLocation: RemoteJob Category: Healthcare/PharmaceuticalsJob SummaryWe are seeking a highly skilled Pharmacovigilance and Safety Specialist to join our team. The successful candidate will be responsible for assessing individual clinical trial and...

  • Clinical Administrative Associate

    3 months ago

    Ridgefield, United States McInnis Inc. Full time

    Job DescriptionJob Description*This Position is onsite in Ridgefield, CT*Currently seeking a Clinical Associate (CA) to join our Study Management & Conduct (SM&C) team located at our Ridgefield, CT facility. The CA will provide administrative operational support to Clinical Operations (CO) for trial-related activities and processes in the operational...

  • Principal / Senior Clinical Data Engineer (SDTM - Data Management)

    1 week ago

    Ridgefield, United States Boehringer Ingelheim Full time

    Description Key contact partner in cultivating the "power of data" by means of (i) data collection/curation, data review, data delivery, (ii) data standardization or (iii) process definition, testing and training. Translate the science into technical specifications. Collect, ingest, structure, curate and standardize all kinds of Clinical Trial related data...

  • Project Management Specialist

    1 month ago

    Ridgefield, Connecticut, United States eTeam Full time

    Project Office SpecialistLocation: HybridContract Duration: 12+ MonthsAs a Project Office Specialist, you will work in close collaboration with the leadership of the Project Office to develop and optimize the new Global CTSU Project Office. Your responsibilities will include the maintenance and enhancement of global CTSU project plan templates within...

  • Project Management Specialist

    4 weeks ago

    Ridgefield, Connecticut, United States eTeam Full time

    Project Office SpecialistLocation: HybridContract Duration: 12+ MonthsAs a Project Office Specialist, you will work in close collaboration with the Head of the Project Office to develop and improve the newly established Global CTSU Project Office. Your responsibilities will include the maintenance and enhancement of global CTSU project plan templates within...

  • Clinical Operations Specialist

    4 months ago

    Ridgefield, United States McInnis Inc. Full time

    Job DescriptionJob DescriptionCurrently, seeking a Clinical Operations Specialist – Technical Support (COS) to join our Business Operations team located at our Ridgefield, CT facility. The COS will provide VBA and SQL programming to existing and new Microsoft Excel workbooks and Microsoft Access databases.  This job is a hybrid position with weekly on...

  • Clinical Operations Manager

    3 weeks ago

    Ridgefield, New Jersey, United States VNS Health Full time

    Job DescriptionVNS Health is seeking a highly skilled and experienced professional to fill the role of Clinical Operations Manager. This position is responsible for overseeing the day-to-day operations of the clinical and non-clinical staff, ensuring efficient and effective delivery of healthcare services.Key Responsibilities:Supervise and Coordinate...

  • Safety and Risk Management Professional

    4 weeks ago

    Ridgefield, Connecticut, United States McInnis Inc. Full time

    Job SummaryMcInnis Inc. is seeking a highly skilled Pharmacovigilance and Safety Specialist to join our team. As a key member of our Pharmacovigilance department, you will be responsible for assessing individual clinical trial and spontaneous case reports for medical review and regulatory reporting determination.Key ResponsibilitiesMedical Review and...

  • Clinical Education Manager

    3 weeks ago

    Ridgefield, New Jersey, United States VNS Health Full time

    About the RoleVNS Health is seeking a highly skilled Clinical Education Manager to join our team. As a key member of our organization, you will be responsible for developing and implementing clinical education programs that foster high-quality care and promote evidence-based practice.Key ResponsibilitiesProgram Development: Design and deliver clinical...

  • Clinical Operations Manager

    3 weeks ago

    Ridgefield, New Jersey, United States VNS Health Full time

    About the RoleVNS Health is seeking a highly skilled Clinical Operations Manager to oversee the day-to-day business operations of our clinical and non-clinical support activities. As a key member of our team, you will be responsible for monitoring internal processes, coordinating activities between clinical and non-clinical staff, and supervising support...

Clinical Trial Manager/site Monitoring

4 months ago

Ridgefield, United States Adientone Full time

Accountable for the execution of monitoring plans & overall quality of monitoring performed by CRAs for assigned US conducted trials (~5-8) across Therapeutic Area(s) phase depending on complexity, size and stage of study.
- Conduct on-site visits to assess CRA performance, including co-monitoring/supervisory visits, as requested, including oversight of CRAs working on assigned trials.
- Implement the monitoring plan as part of the Trial Team. Monitor clinical monitoring deliverables for assigned trials in clinical operations system(s)(e.g. BI CTMS).
- Deliver Risk-based Site Monitoring approach and local training for the trial.
- Develop and provide appropriate training of local trial teams (e.g. Clinical Trial Managers (CT Manager) and Clinical Research Associates (CRA)).
- Assist with in-house Site Monitoring inspection readiness activities and lead preparation for US site regulatory inspections, as requested.
- Behave as local expert and consultant on site management and monitoring topics.
- Participate in and contribute to global/regional and local Trial Team meetings, international/ regional / local Investigator Meetings.
- Timely responses to Site Management and monitoring questions from external and internal stakeholders (including Regulatory Authority/Ethics Committee).

Trial Conduct:
Monitor progress and oversee Site Management and Monitoring activities conducted by CRO partners during clinical trial conduct including adherence to ICH-GCP, and regulatory requirements, compliance with SOPs, trial protocol, trial quality management and Site Monitoring plans.

Including but not limited to:

- Issue management / oversight on country level.
- Continuous review, risk identification, evaluation/ analysis and communication on a country level as applicable.
- Maintain Risk-based Site Monitoring approach for the OPU and provide feedback on the trends identified that may impact the TLMM and/or site monitoring oversight plan.
- Conduct Site and Monitoring Oversight (including Site Monitoring Oversight Visits) at OPU according to plan, implement follow-up actions and escalation, as required.
- In conjunction with SML-r, contribute to preparation and implementation of trial level documents including training material updates/retraining as needed.
- In conjunction with SML-r, facilitate communication and training related to site monitoring in the trial at the OPU:
Communication and training of CT Managers and CRAs. Performing re
- training as necessary.
- Participate, prepare input (as requested by SML-r) for Trial Oversight Meetings (country level) and contribute to the timely responses to questions from external and internal stakeholders.

**Skills**:Oncology experience

metabolic experience

Dermatology experince

CNS experiecne

Keywords:
Education: Bachelor's Degree (Health Sciences, Health Care, Nursing or Others) required with a minimum of 5 years of experience performing on-site monitoring or 8 years of relevant business experience in the regulated pharmaceutical or healthcare industry, including on-site monitoring experience.

Skills and Experience:
**Required Skills**:
PROJECT MANAGEMENT

CAPA

RISK ASSESSMENT

CLINICAL TRIAL MONITORING

DERMATOLOGICAL

Additional Skills:
CLINICAL SITE MONITORING

ONCOLOGY

CLINICAL MONITORING

Languages:
English

Read

Write

Speak

Minimum Degree Required: Bachelor's Degree

**Job Type**: Contract

Pay: $3,200.00 - $3,500.00 per week

Schedule:

- 8 hour shift
- Day shift
- Monday to Friday

Ability to Relocate:

- Ridgefield, CT: Relocate before starting work (required)

Work Location: On the road