Jobs
Jobs
35,006 jobs found
Loading more...
The Goodyear Tire & Rubber Company
Service Manager - Hazelwood, MO
Source: National Labor Exchange
Burns & McDonnell
Program Manager - Transmission & Distribution (Kansas City/Omaha)
Source: National Labor Exchange
Meta
Construction Manager - Data Center Design, Engineering and Construction
Source: National Labor Exchange
Accenture
Technology Strategy Manager/Sr Manager, Financial Services
Source: National Labor Exchange
Walmart
eCom Warehouse Worker
Source: National Labor Exchange
BJC HealthCare
New Graduate Nurse at Progress West Hospital
Source: National Labor Exchange
BJC HealthCare
New Graduate Nurse at Barnes-Jewish St. Peters Hospital
Source: National Labor Exchange
HCA Healthcare
Occupational Therapist Inpatient
Source: National Labor Exchange
Walmart
Orderfiller / Loader / Unloader
Source: National Labor Exchange
Walmart
Freight Handler
Source: National Labor Exchange
Walmart
Power Equipment Operator
Source: National Labor Exchange
Wipfli Advisory LLC
Senior Manager, Accounting Advisory - Skilled Nursing Industry Clients
Source: National Labor Exchange
Wipfli Advisory LLC
Manager, Accounting Advisory - Skilled Nursing Industry Clients
Source: National Labor Exchange
SSM Health
Registered Nurse - Charge Nurse
Source: National Labor Exchange
SSM Health
Coder II - Professional
Source: National Labor Exchange
CenterWell
Primary Care Physician
Source: National Labor Exchange
HCA Healthcare
Family Medicine Physician
Source: National Labor Exchange
HCA Healthcare
Registered Nurse RN Progressive Care
Source: National Labor Exchange
Evolent
Software Engineer
Source: National Labor Exchange
BJC HealthCare
New Graduate Nurse at BJC HealthCare
Source: National Labor Exchange
Walmart
Online Order Filling Team Supervisor
Source: National Labor Exchange
Affordable Care
Dental Assistant
Source: National Labor Exchange
Walmart
Independent Optometrist - Walmart
Source: National Labor Exchange
Olsson
Senior Construction Materials Testing Technician (Travel Required)
Source: National Labor Exchange
Parexel
Clinical Study Physician - Oncology - FSP
Source: National Labor Exchange
Accenture
Investment Banking Manager
Source: National Labor Exchange
Papa John's International
Manager Designate
Source: National Labor Exchange
Papa John's International
Shift Leader
Source: National Labor Exchange
Papa John's International
Restaurant Team Member
Source: National Labor Exchange
Papa John's International
Delivery Driver
Source: National Labor Exchange
Burns & McDonnell
Energy & Utilities Analyst - 1898 & Co., Power Systems Planning - Electrical (Kansas City)
Source: National Labor Exchange
ProEnergy
Parts Prep Operator- 3rd Shift
Source: MO Jobs
Jacobs
Electrical Engineer
Source: National Labor Exchange
Labcorp
South Central Region - Venipuncture/Biometric Screener Wellness Worker
Source: National Labor Exchange
Walmart
Pharmacy Operations Team Lead
Source: National Labor Exchange
Walmart
Pharmacy Operations Team Lead
Source: National Labor Exchange
MLC
Heavy Equipment Operator - Underground
Source: National Labor Exchange
State of Missouri
Clinical Caseworker, Senior Clinical Caseworker, LMSW, LCSW RSM
Source: MO Careers
General Dynamics Information Technology
Lead Firearms Instructor - Part Time / on Call
Source: National Labor Exchange
Burns & McDonnell
Grid Systems - Sr. Solution Architect
Source: National Labor Exchange
Loading more...
Job ID #103280
Parexel
Clinical Study Physician - Oncology - FSP
location_on
Jefferson City, MO
description
Summary
Parexel FSP has an exciting opportunity for a Clinical Study Physician. This is a fully remote role! Oncology experience needed
External Job Description
The Study Physician (SP) is a critical global role that is created to take up medical responsibilities of clinical trials within Clinical Development & Operations by a qualified and clinically experienced physician. The SP is medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trial. During the clinical trial, SP is responsible to provide state-of-the-art medical expertise to fully execute medical oversight from the Trial Design Outline (TDO) kick off to the Clinical Trial Report (CTR). SP is a core member of the Trial Team and the Evidence Network Team.
Trial Start-Up
+ Responsible for medical content of Clinical Trial Protocols (CTPs), in line with TDO, in collaboration with the Clinical Trial Lead (CTL), Clinical Program Lead (CPL), Patient Safety Physician, Medical Writer and other trial and evidence team members to ensure high medical quality CTP. Medical input into CTP updates.
+ Contribution to trial risk-based quality management from medical perspective, by defining medically relevant critical data/processes, related risks, and its mitigation/monitoring strategies in the Integrated Quality and Risk Management Plan (IQRMP) as well as in risk discussions during trial conduct.
+ Medical responsibility as co-author for the development of a robust Clinical Quality Monitoring Plan (CQMP) in line with the critical data, medical quality risks and related monitoring/ mitigations identified in IQRMP.
+ Responsible for providing medical input into the definition of important protocol deviations (iPD), providing input for compilation and review of trial iPD list from medical perspective, and support trial team in deciding on iPDs from identified potential iPDs.
+ Contribution to the timely preparation of medically relevant core trial documents and timely milestones.
+ Medical input into Data Management documentation for the trial, such as eCRF design by efficient translation of medical questions into electronic data capturing, "Information for CRF completion" (ICC), Data Review Plan (e.g.,propose items such as data screening rules for automated data queries, automated or manual data checks for clinical data consistency), laboratory parameters specifications for the project, Data Transfer Agreement, central laboratory alerts.
+ Responsible for the medical content of Patient Information and Informed Consent, Trial Level Monitoring Manual, Trial Communication Plan, Trial Training Plan, and Trial Statistical Analysis Plan.
+ Medical contribution to Patient Narrative preparation, Clinical Trial Report planning and review of medical sections of Clinical Trial Report
+ Contribute to the medical content of responses to questions from regulators and Ethic Committees/IRBs.
+ Medical input to study and site feasibility in planning and execution, patient recruitment, and retention plans.
+ Provision of medical training at Country feasibility training, Trial Investigators Meetings or to Sponsor staff.
Trial Conduct
+ Ongoing medical review with transparent documentation of the activity, related findings and resolutions.
+ Execution of relevant clinical quality monitoring for Study Physician using aggregated data outputs as per trial CQMP, timely mitigation & escalation of identified risks & quality issues.
+ Responsibility for agile and adaptive risk based Clinical Quality Monitoring of critical data. Support close to real time clinical data medical oversight by using advanced technologies and systems.
+ Proactively address/ communicate clinical quality issues in a collaborative environment.
+ Early and fast recognition of inconsistencies of medical data and practical difficulties in execution of study protocols
+ Respond to medical queries from Investigators, CROs, and/or Sponsor team representatives and contribute to the maintenance of trial FAQ log/list.
+ Building network with experts and active contribution to site engagement.
+ Support Endpoint Adjudication (EA), Data Monitoring Committee (DMC), Data Safety Monitoring Boards (DSMB) and Steering Committees (SC) (as applicable), by presenting medical content of study to the respective committees, responding to medical questions and by ensuring good quality of data from CQM.
+ Medical review of and contribution to the content of Trial Newsletters
+ Contribution to the scientific publication of trial data, if applicable
Leadership
+ Management of medical activities related to one or more clinical trials
+ Cross functional planning, execution, and analysis of a clinical program
+ Responsible for medical assessments, decisions and medical quality for individual trials, assets and client processes
Compliance with Parexel standards
+ Comply with required training curriculum
+ Complete timesheets accurately and timely as required
+ Submit expense reports as required
+ Update CV as required
+ Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements
Skills:
+ Proficiency with Windows, MS Office (Word, PowerPoint, Excel, Outlook)
+ Proficiency in written and spoken English and (local language)
+ Excellent interpersonal, active listening and influencing skills
+ Pronounced analytical skills and systematic and well-structured working style.
+ Pronounced presentation and training skills
+ Capability to work proactively and with team spirit in an international environment
+ Ability to use digital technologies to access information, be creative, innovate, solve problems, communicate, navigate, learn & apply in a digital environment
Knowledge and Experience :
+ Experience in the pharma industry or CRO in medical, project management or global pharmacovigilance functions/any other relevant medical function, ideally in Clinical Development, with required capabilities
+ Understanding of relevant regulations and guidance including ICH-GCP.
+ Experienced with data visualization systems and IT systems.
Education:
+ Physician MD, ideally with medical thesis, trained in a clinical setting
+ Minimum of 4 years of active clinical experience; specialization in internal medicine or general practice preferred.
\#LI-LG4
\#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
External Job Description
The Study Physician (SP) is a critical global role that is created to take up medical responsibilities of clinical trials within Clinical Development & Operations by a qualified and clinically experienced physician. The SP is medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trial. During the clinical trial, SP is responsible to provide state-of-the-art medical expertise to fully execute medical oversight from the Trial Design Outline (TDO) kick off to the Clinical Trial Report (CTR). SP is a core member of the Trial Team and the Evidence Network Team.
Trial Start-Up
+ Responsible for medical content of Clinical Trial Protocols (CTPs), in line with TDO, in collaboration with the Clinical Trial Lead (CTL), Clinical Program Lead (CPL), Patient Safety Physician, Medical Writer and other trial and evidence team members to ensure high medical quality CTP. Medical input into CTP updates.
+ Contribution to trial risk-based quality management from medical perspective, by defining medically relevant critical data/processes, related risks, and its mitigation/monitoring strategies in the Integrated Quality and Risk Management Plan (IQRMP) as well as in risk discussions during trial conduct.
+ Medical responsibility as co-author for the development of a robust Clinical Quality Monitoring Plan (CQMP) in line with the critical data, medical quality risks and related monitoring/ mitigations identified in IQRMP.
+ Responsible for providing medical input into the definition of important protocol deviations (iPD), providing input for compilation and review of trial iPD list from medical perspective, and support trial team in deciding on iPDs from identified potential iPDs.
+ Contribution to the timely preparation of medically relevant core trial documents and timely milestones.
+ Medical input into Data Management documentation for the trial, such as eCRF design by efficient translation of medical questions into electronic data capturing, "Information for CRF completion" (ICC), Data Review Plan (e.g.,propose items such as data screening rules for automated data queries, automated or manual data checks for clinical data consistency), laboratory parameters specifications for the project, Data Transfer Agreement, central laboratory alerts.
+ Responsible for the medical content of Patient Information and Informed Consent, Trial Level Monitoring Manual, Trial Communication Plan, Trial Training Plan, and Trial Statistical Analysis Plan.
+ Medical contribution to Patient Narrative preparation, Clinical Trial Report planning and review of medical sections of Clinical Trial Report
+ Contribute to the medical content of responses to questions from regulators and Ethic Committees/IRBs.
+ Medical input to study and site feasibility in planning and execution, patient recruitment, and retention plans.
+ Provision of medical training at Country feasibility training, Trial Investigators Meetings or to Sponsor staff.
Trial Conduct
+ Ongoing medical review with transparent documentation of the activity, related findings and resolutions.
+ Execution of relevant clinical quality monitoring for Study Physician using aggregated data outputs as per trial CQMP, timely mitigation & escalation of identified risks & quality issues.
+ Responsibility for agile and adaptive risk based Clinical Quality Monitoring of critical data. Support close to real time clinical data medical oversight by using advanced technologies and systems.
+ Proactively address/ communicate clinical quality issues in a collaborative environment.
+ Early and fast recognition of inconsistencies of medical data and practical difficulties in execution of study protocols
+ Respond to medical queries from Investigators, CROs, and/or Sponsor team representatives and contribute to the maintenance of trial FAQ log/list.
+ Building network with experts and active contribution to site engagement.
+ Support Endpoint Adjudication (EA), Data Monitoring Committee (DMC), Data Safety Monitoring Boards (DSMB) and Steering Committees (SC) (as applicable), by presenting medical content of study to the respective committees, responding to medical questions and by ensuring good quality of data from CQM.
+ Medical review of and contribution to the content of Trial Newsletters
+ Contribution to the scientific publication of trial data, if applicable
Leadership
+ Management of medical activities related to one or more clinical trials
+ Cross functional planning, execution, and analysis of a clinical program
+ Responsible for medical assessments, decisions and medical quality for individual trials, assets and client processes
Compliance with Parexel standards
+ Comply with required training curriculum
+ Complete timesheets accurately and timely as required
+ Submit expense reports as required
+ Update CV as required
+ Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements
Skills:
+ Proficiency with Windows, MS Office (Word, PowerPoint, Excel, Outlook)
+ Proficiency in written and spoken English and (local language)
+ Excellent interpersonal, active listening and influencing skills
+ Pronounced analytical skills and systematic and well-structured working style.
+ Pronounced presentation and training skills
+ Capability to work proactively and with team spirit in an international environment
+ Ability to use digital technologies to access information, be creative, innovate, solve problems, communicate, navigate, learn & apply in a digital environment
Knowledge and Experience :
+ Experience in the pharma industry or CRO in medical, project management or global pharmacovigilance functions/any other relevant medical function, ideally in Clinical Development, with required capabilities
+ Understanding of relevant regulations and guidance including ICH-GCP.
+ Experienced with data visualization systems and IT systems.
Education:
+ Physician MD, ideally with medical thesis, trained in a clinical setting
+ Minimum of 4 years of active clinical experience; specialization in internal medicine or general practice preferred.
\#LI-LG4
\#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Do You Have a MO Jobs Account?
Your HireMO account is created from your MO Jobs account, so we need to connect the two.
Already have an account?
Sign In
First, Let's Find Your MO Jobs Account
HireMO works together with MO Jobs, the State of Missouri jobs website.
Create an Account to Apply
Your MO Jobs account is connected. Choose an email and password to sign in to HireMO.
You Need a MO Jobs Account First
HireMO works together with MO Jobs, the State of Missouri jobs website. You need a MO Jobs account before you can create your HireMO account.
- Create your MO Jobs account at jobs.mo.gov. It is free.
- Log in to MO Jobs, then click HireMO from there. That link brings you back here to finish your registration.
- Complete your HireMO account.