Medical Writing Operation Associate The primary purpose of this job is to provide support for ... of the TMF. 60% Contract management; responsible for initiating contract renewals with MW ...
Medical Writing Operation Associate The primary purpose of this job is to provide support for ... of the TMF. 60% Contract management; responsible for initiating contract renewals with MW ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
Quick apply
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Clinical Trial Manager
Boston, MA · On-site
Responsible for maintaining internal study documents in the Trial Master File (TMF) and ... Strong interpersonal skills with the ability to interact effectively with all levels of associates ...
Clinical Trial Manager
Boston, MA · On-site
Responsible for maintaining internal study documents in the Trial Master File (TMF) and ... Strong interpersonal skills with the ability to interact effectively with all levels of associates ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
Quick apply
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
Clinical Trial Associate
Waltham, MA · On-site
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Support Trial Master File (TMF) activities, including document filing and quality control checks ...
Clinical Trial Associate
Waltham, MA · On-site
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Support Trial Master File (TMF) activities, including document filing and quality control checks ...
Clinical Trial Associate
Waltham, MA · On-site
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Support Trial Master File (TMF) activities, including document filing and quality control checks ...
Clinical Trial Associate
Waltham, MA · On-site
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Support Trial Master File (TMF) activities, including document filing and quality control checks ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation ...
The Associate Director will also work collaboratively across the therapeutic area and cross ... Oversee or conduct routine completeness checks of the Trial Master File (TMF) to ensure compliance ...
The Associate Director will also work collaboratively across the therapeutic area and cross ... Oversee or conduct routine completeness checks of the Trial Master File (TMF) to ensure compliance ...
Clinical Study Specialist
Cambridge, MA · On-site
... Leads, Clinical Study Associate Managers, CROs, and study sites. This position offers the ... Ensures timely receipt of scheduled reports (e.g., 1572s, financial disclosures) and performs TMF ...
Clinical Study Specialist
Cambridge, MA · On-site
... Leads, Clinical Study Associate Managers, CROs, and study sites. This position offers the ... Ensures timely receipt of scheduled reports (e.g., 1572s, financial disclosures) and performs TMF ...
Senior Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
We are seeking a detail-oriented and proactive Senior Clinical Trial Associate (Sr. CTA) to support ... Support Trial Master File (TMF) management, including document filing and quality control * Assist ...
Senior Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
We are seeking a detail-oriented and proactive Senior Clinical Trial Associate (Sr. CTA) to support ... Support Trial Master File (TMF) management, including document filing and quality control * Assist ...
Clinical Trial Associate II
Cambridge, MA · On-site
$36.50 - $50/hr
The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... Support the establishment and maintenance of the study TMF. Prepare master Clinical Study Files and ...
Clinical Trial Associate II
Cambridge, MA · On-site
$36.50 - $50/hr
The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... Support the establishment and maintenance of the study TMF. Prepare master Clinical Study Files and ...
Clinical Research Associate (CRA) - Temporary Location: Waltham, MA Schedule: Flexible hours, about ... Maintain accurate and timely Trial Master File (TMF) documentation and study records. * Track and ...
Clinical Research Associate (CRA) - Temporary Location: Waltham, MA Schedule: Flexible hours, about ... Maintain accurate and timely Trial Master File (TMF) documentation and study records. * Track and ...
Senior Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
We are seeking a detail-oriented and proactive Senior Clinical Trial Associate (Sr. CTA) to support ... Support Trial Master File (TMF) management, including document filing and quality control * Assist ...
Senior Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
We are seeking a detail-oriented and proactive Senior Clinical Trial Associate (Sr. CTA) to support ... Support Trial Master File (TMF) management, including document filing and quality control * Assist ...
The Associate Director will also work collaboratively across the therapeutic area and cross ... Oversee or conduct routine completeness checks of the Trial Master File (TMF) to ensure compliance ...
The Associate Director will also work collaboratively across the therapeutic area and cross ... Oversee or conduct routine completeness checks of the Trial Master File (TMF) to ensure compliance ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Quick apply
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Clinical Research Associate (CRA) - Temporary Location: Waltham, MA Schedule: Flexible hours, about ... Maintain accurate and timely Trial Master File (TMF) documentation and study records. * Track and ...
Quick apply
Clinical Research Associate (CRA) - Temporary Location: Waltham, MA Schedule: Flexible hours, about ... Maintain accurate and timely Trial Master File (TMF) documentation and study records. * Track and ...
Associate Director, Clinical Supply Chain
Waltham, MA · On-site
$196K - $222K/yr
The Associate Director position within Clinical Supply Chain provides strategic leadership and ... Ensure timely and accurate updates to Trial Master Files (TMF) with essential supply chain ...
Associate Director, Clinical Supply Chain
Waltham, MA · On-site
$196K - $222K/yr
The Associate Director position within Clinical Supply Chain provides strategic leadership and ... Ensure timely and accurate updates to Trial Master Files (TMF) with essential supply chain ...
The Global Monitoring Manager / Associate Director (GMM/AD) leads and oversees clinical monitoring ... Maintain inspection readiness of the Trial Master File (TMF) and monitoring documentation at all ...
The Global Monitoring Manager / Associate Director (GMM/AD) leads and oversees clinical monitoring ... Maintain inspection readiness of the Trial Master File (TMF) and monitoring documentation at all ...
Tmf Associate information
See Boston, MA salary details
$18.80 - $24.02
4% of jobs
$24.02 - $29.25
8% of jobs
$29.25 - $34.47
12% of jobs
$34.63 is the 25th percentile. Wages below this are outliers.
$34.47 - $39.69
26% of jobs
$39.69 - $44.92
18% of jobs
$46.73 is the 75th percentile. Wages above this are outliers.
$44.92 - $50.14
19% of jobs
$50.14 - $55.36
6% of jobs
$55.36 - $60.58
2% of jobs
$60.58 - $65.81
1% of jobs
$65.81 - $71.03
1% of jobs
$71.03 - $76.25
2% of jobs
$18
$43
$76
How much do tmf associate jobs pay per hour?
What is the difference between Tmf Associate vs Tmf Analyst?
| Aspect | Tmf Associate | Tmf Analyst |
|---|---|---|
| Required Credentials | Bachelor's degree in life sciences, pharmacy, or related fields; basic knowledge of clinical trial processes | Bachelor's or master's degree; deeper understanding of TMF processes and regulatory requirements |
| Work Environment | Clinical research organizations, pharmaceutical companies, or CROs; supporting TMF documentation | More analytical role within similar settings; involved in reviewing and ensuring compliance |
| Employer & Industry Usage | Commonly used in clinical trial documentation teams | Used in quality assurance and compliance teams within the same industry |
The main difference between a Tmf Associate and a Tmf Analyst lies in their experience level and scope of responsibilities. Tmf Associates typically handle documentation support and basic compliance tasks, while Tmf Analysts perform more detailed reviews and analysis to ensure regulatory adherence. Both roles are essential in clinical trial management, with the Analyst position requiring a deeper understanding of TMF processes.
What are the most commonly searched types of Tmf jobs in Boston, MA?
The most popular types of Tmf jobs in Boston, MA are:
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For Tmf Associate jobs in Boston, MA, the most frequently searched job titles are:
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The top searched job categories for Tmf Associate jobs in Boston, MA are:
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Cities near Boston, MA with the most Tmf Associate job openings:

Contractor
Re-posted 10 days ago
Job description
A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Title : Medical Writing Operation Associate
The primary purpose of this job is to provide support for contracts, PDP resourcing, and document finalization and filing.Â
Assist Medical Writing Operations staff with document approval and notification processes and filing/QC of the TMF. 60%Â
Contract management; responsible for initiating contract renewals with MW functional service providers and partners, including negotiations/follow-up with vendors, ensuring appropriate signatures are obtained, ensuring purchase orders are in place, and filing final, fully executed contracts in Selectica. 10%Â
Managing resourcing and capacity estimates in PDP for MW function. 10%Â
Assist Medical Writing staff with document formatting/troubleshooting/reference management 20%Â
Advanced Microsoft Office skills (Word, PowerPoint, Excel); able to use Adobe, Documentum, other systems (internal systems: Selectica, PDP, BRASS, RADAR, PhIL), as needed.Â
Contract negotiation experience/familiarity with contract languageÂ
Strong attention to detailÂ
Ability to multitask in a fast-paced environmentÂ
Excellent oral and written communication skillsÂ
Aptitude for learning new systems and technologyÂ
Familiarity with the clinical development process a plusÂ
Bachelor's Degree requiredÂ
Archana Melwani
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Inc. 5000 - 2007-2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
Tel: 732-549-2030 x130
Direct: 732-429-1853
Fax: 732-549-5549
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996