Jobs
Jobs
35,007 jobs found
Loading more...
BUNZL
Market Purchasing Manager
Source: National Labor Exchange
BUNZL
Office Manager
Source: National Labor Exchange
BUNZL
Warehouse Worker
Source: National Labor Exchange
BIG SPRINGS MEDICAL ASSOCIATION INC.
LCSW or LPC - Viburnum, MO
Levi, Ray & Shoup, Inc.
Full Stack Engineer
Source: National Labor Exchange
Levi, Ray & Shoup, Inc.
.Net Developer
Source: National Labor Exchange
AT&T
Assistant Store Manager
Source: National Labor Exchange
PEPSICO
Merchandiser - Beverages
Sodexo
Concessions Worker
Source: National Labor Exchange
Sodexo
Stock Worker and Receiver
Source: National Labor Exchange
Sodexo
Cook II
Source: National Labor Exchange
Sodexo
Maintenance, Operations and Quality Program Manager
Source: National Labor Exchange
Sodexo
Materials Delivery Worker
Source: National Labor Exchange
Sodexo
Facilities Lead Worker
Source: National Labor Exchange
Sodexo
Dishroom Attendant
Source: National Labor Exchange
Sodexo
Steward
Source: National Labor Exchange
Sodexo
Stock Worker and Receiver
Source: National Labor Exchange
Sodexo
Cook II
Source: National Labor Exchange
Sodexo
Student Worker
Source: National Labor Exchange
Sodexo
Food Supervisor
Source: National Labor Exchange
Sodexo
Cashier/Food Service Worker
Source: National Labor Exchange
Sodexo
Dishwasher
Source: National Labor Exchange
Sodexo
Food Service Worker
Source: National Labor Exchange
Sodexo
Dietitian Nutritionist II - Healthcare
Source: National Labor Exchange
Sodexo
Housekeeping Attendant
Source: National Labor Exchange
Dollar Tree
Merchandising Assistant Manager
Source: National Labor Exchange
Dollar Tree
Store Manager
Source: National Labor Exchange
Dollar Tree
Assistant Manager I
Source: National Labor Exchange
Dollar Tree
Assistant Manager I
Source: National Labor Exchange
Dollar Tree
Store Manager
Source: National Labor Exchange
Merck
Associate Director Account Management
Source: National Labor Exchange
Merck
Territory Sales Manager, Beef Monitoring - Texas Panhandle, Southwest Kansas, New Mexico
Source: National Labor Exchange
Merck
Senior Companion Animal Territory Representative - (Delaware/ Maryland Eastern Shore)
Source: National Labor Exchange
Merck
Clinical Trial Coordinator (CTC) - Remote
Source: National Labor Exchange
Merck
Territory Sales Manager, Beef Monitoring (TX or LA Based)
Source: National Labor Exchange
Merck
Clinical Trial Coordinator - Monitoring (Remote)
Source: National Labor Exchange
Merck
Regional Medical Scientific Director (US Medical Affairs) Immunology - Gastrointestinal (Southern Midwest)
Source: National Labor Exchange
Merck
Senior Clinical Trial Coordinator (Sr. CTC) - Remote
Source: National Labor Exchange
Ford Motor Company
Global TA Operations Program Lead
Source: National Labor Exchange
Ford Motor Company
STA Technical Specialist - Electronics
Source: National Labor Exchange
Loading more...
Job ID #105897
Merck
Clinical Trial Coordinator (CTC) - Remote
location_on
Jefferson City, MO
description
Summary
Job Description
Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.
The role is critical to meet planned Site Ready dates, including assisting with the preparation of submission packages to IRB/ERC and Health Authorities. The role will collaborate at local level closely with COM, CRM and CRA. And the person collaborates with finance/budgeting representatives to manage CTRAs and payments.
Responsibilities include, but are not limited to:
Trial and site administration:
+ Track (e.g. essential documents) and report (e.g. Safety Reports).
+ Ensure collation and distribution of study tools and documents.
+ Update clinical trial databases (CTMS) and trackers.
+ Clinical supply & non-clinical supply management, in collaboration with other country roles.
+ Manage Labeling requirements and coordinate/sign translation change request, in collaboration with other country roles (if applicable).
Document management:
+ Prepare documents and correspondence.
+ Collate, distribute/ship, and archive clinical documents, e.g. eTMF.
+ Assist with eTMF reconciliation.
+ Execute eTMF Quality Control Plan.
+ Update manuals/documents (e.g., patient diaries, instructions).
+ Document proper destruction of clinical supplies.
+ Prepare Investigator trial file binders.
+ Obtain translations of documents.
Regulatory & Site Start-Up responsibilities: Collaborate with other country roles to:
+ In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions.
+ Obtain, track and update study insurance certificates.
+ Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.
+ Publish study results for GCTO and RA where required per local legislation.
Budgeting, Agreement and Payments:
Collaborate with finance/budgeting representatives for:
+ Develop, control, update and close-out country and site budgets (including Split site budget).
+ Develop, negotiate, approve and maintain contracts (e.g. CTRAs).
+ Track and report contract negotiations.
+ Update and maintain contract templates (in cooperation with Legal Department).
+ Calculate and execute payments (to investigators, vendors, grants).
+ Ensure adherence to financial and compliance procedures.
+ Monitor and track adherence and disclosures.
+ Maintain tracking tools.
+ Obtain and process FCPA documentation in a timely manner.
Meeting Planning:
+ Organize meetings (create & track study memos/letters/protocols).
+ Support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable).
Skills:
+ Fluent in Local Languages and business proficient in English (verbal and written) and excellent communication skills.
+ Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.
+ Hands on knowledge of Good Documentation Practices.
+ Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt to new IT applications. Strong MS Excel skills required.
+ ICH-GCP Knowledge appropriate to role.
+ Excellent negotiation skills for CTCs in finance area.
+ Effective time management, organizational and interpersonal skills, conflict management.
+ Effective communication with external customers (e.g. sites and investigators)
+ High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.
+ Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.
+ Demonstrates commitment to Customer focus, both internally and externally.
+ Able to work independently.
+ Proactive attitude to solving problems / proposing solutions.
+ Positive mindset, growth mindset.
Qualification & Experience:
+ Completed job training (office management, administration, finance, health care preferred) or Bachelor's Degree.
_\#MSJR_
\#eligibleforERP
\#clinicaltrialjobs
_The salary range for this role is:_ $68,000 - $107,000
_This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs._
_ _
_The successful candidate will be eligible for annual bonus and long-term incentive, if applicable._
_ _
_We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days._
Required Skills:
Clinical Document Management, Clinical Research, Clinical Trial Documentation, Clinical Trial Management, Clinical Trials Monitoring, Clinical Trials Operations, Clinical Trial Support, Customer-Focused, Microsoft Excel, Microsoft Office
Preferred Skills:
Clinical Trial Management Systems (CTMS), Clinical Trials, Communication
Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)
Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf)
EEOC GINA Supplement
We are proud to be a company that embraces the value...
Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.
The role is critical to meet planned Site Ready dates, including assisting with the preparation of submission packages to IRB/ERC and Health Authorities. The role will collaborate at local level closely with COM, CRM and CRA. And the person collaborates with finance/budgeting representatives to manage CTRAs and payments.
Responsibilities include, but are not limited to:
Trial and site administration:
+ Track (e.g. essential documents) and report (e.g. Safety Reports).
+ Ensure collation and distribution of study tools and documents.
+ Update clinical trial databases (CTMS) and trackers.
+ Clinical supply & non-clinical supply management, in collaboration with other country roles.
+ Manage Labeling requirements and coordinate/sign translation change request, in collaboration with other country roles (if applicable).
Document management:
+ Prepare documents and correspondence.
+ Collate, distribute/ship, and archive clinical documents, e.g. eTMF.
+ Assist with eTMF reconciliation.
+ Execute eTMF Quality Control Plan.
+ Update manuals/documents (e.g., patient diaries, instructions).
+ Document proper destruction of clinical supplies.
+ Prepare Investigator trial file binders.
+ Obtain translations of documents.
Regulatory & Site Start-Up responsibilities: Collaborate with other country roles to:
+ In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions.
+ Obtain, track and update study insurance certificates.
+ Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.
+ Publish study results for GCTO and RA where required per local legislation.
Budgeting, Agreement and Payments:
Collaborate with finance/budgeting representatives for:
+ Develop, control, update and close-out country and site budgets (including Split site budget).
+ Develop, negotiate, approve and maintain contracts (e.g. CTRAs).
+ Track and report contract negotiations.
+ Update and maintain contract templates (in cooperation with Legal Department).
+ Calculate and execute payments (to investigators, vendors, grants).
+ Ensure adherence to financial and compliance procedures.
+ Monitor and track adherence and disclosures.
+ Maintain tracking tools.
+ Obtain and process FCPA documentation in a timely manner.
Meeting Planning:
+ Organize meetings (create & track study memos/letters/protocols).
+ Support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable).
Skills:
+ Fluent in Local Languages and business proficient in English (verbal and written) and excellent communication skills.
+ Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.
+ Hands on knowledge of Good Documentation Practices.
+ Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt to new IT applications. Strong MS Excel skills required.
+ ICH-GCP Knowledge appropriate to role.
+ Excellent negotiation skills for CTCs in finance area.
+ Effective time management, organizational and interpersonal skills, conflict management.
+ Effective communication with external customers (e.g. sites and investigators)
+ High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.
+ Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.
+ Demonstrates commitment to Customer focus, both internally and externally.
+ Able to work independently.
+ Proactive attitude to solving problems / proposing solutions.
+ Positive mindset, growth mindset.
Qualification & Experience:
+ Completed job training (office management, administration, finance, health care preferred) or Bachelor's Degree.
_\#MSJR_
\#eligibleforERP
\#clinicaltrialjobs
_The salary range for this role is:_ $68,000 - $107,000
_This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs._
_ _
_The successful candidate will be eligible for annual bonus and long-term incentive, if applicable._
_ _
_We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days._
Required Skills:
Clinical Document Management, Clinical Research, Clinical Trial Documentation, Clinical Trial Management, Clinical Trials Monitoring, Clinical Trials Operations, Clinical Trial Support, Customer-Focused, Microsoft Excel, Microsoft Office
Preferred Skills:
Clinical Trial Management Systems (CTMS), Clinical Trials, Communication
Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)
Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf)
EEOC GINA Supplement
We are proud to be a company that embraces the value...
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.