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Proposal Manager Clinical Trials Jobs (NOW HIRING)

Natera

Manager, Clinical Trials

OR · On-site +1

The Manager, Clinical Trials will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects ...

Natera

Manager, Clinical Trials

$115K - $144K/yr

The Manager, Clinical Trials will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects ...

HonorHealth

Manager - Clinical Trials

Scottsdale, AZ · On-site

... all trials within the portfolio, escalating concerns and issues to the HRI operational and ... Manager is the facilitator for clinical communication between the program, leadership, and the ...

Honorhealth

Manager - Clinical Trials

Scottsdale, AZ · On-site

... all trials within the portfolio, escalating concerns and issues to the HRI operational and ... Manager is the facilitator for clinical communication between the program, leadership, and the ...

Natera

Senior Manager, Clinical Trials

OR · On-site +1

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests.

Careerxchange

Operations Manager Clinical Trials

Miami, FL · On-site

$41 - $56/hr

Monday - Friday | 8:30 AM - 5:00 PM Pay: $41.00 - $56.00 per hour Job Summary We are seeking an experienced Clinical Trials Operations Manager to support a leading clinical research program during a ...

Natera

Senior Manager, Clinical Trials

$141K - $176K/yr

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests.

Washington University of St. Louis

$75K - $128K/yr

Skills: Clinical Project Management, Clinical Systems, Clinical Trials Administration, Deadline Management, Interpersonal Relationships, Leadership, Microsoft Excel, Microsoft Word, Oral ...

New

Washington University of St. Louis

The selected candidate will work collaboratively and directly with the Center for Clinical Theranostics Research (CCTR) managing radiopharmaceutical clinical trials led by Dr. Wahl. The relevant ...

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Proposal Manager Clinical Trials information

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$30.5K

$99.5K

$143K

How much do proposal manager clinical trials jobs pay per year?

As of Sep 11, 2026, the average yearly pay for proposal manager clinical trials in the United States is $99,490.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,500.00 and $118,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Proposal Manager Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $99,490 per year, or $47.8 per hour.

Manager, Clinical Trials

OR • On-site, Remote

Natera
Biotechnology Research and Development • 1 - 5K employees
Learn more about Nateraexternal

Full-time

Posted 23 days ago

Natera rating

7.8

Company rating: 7.8 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

Job description

POSITION SUMMARY:

The Manager, Clinical Trials will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, and is expected to provide functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements.

PRIMARY RESPONSIBILITIES:

  • Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met

  • Responsible for selection of vendors/CROs and provide effective ongoing management to vendors/CROs working on the project to ensure compliance and execution of project deliverables within the approved budget, study timeline, and study protocol. Works closely with investigative site personnel, CROs, and other study vendors

  • Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites

  • Lead study-related activities such as protocol and informed consent preparation, investigator selection, study training material development and delivery, monitoring plans development and execution, CRFs, design and completion, TMF maintenance, protocol amendment and clinical report preparation, as required

  • Collaborate with Clinical Data Management group to ensure correct CRFs content is collected, prepare comprehensive completion guidelines, and design effective data listings and study reports

  • Train CROs, vendors, investigators and study coordinators on implementation of study protocol

  • Hire, train, manage and oversee Clinical trial staff, and serve as a resource for others within the company for clinical trials management expertise

  • Monitor and track clinical trial progress and provide status update to stakeholders

  • Support sample management and prospective sample testing for studies where Natera functions as a central testing facility

  • Partner with other research and development groups to create a culture of mutual respect and focus on delivery of high-quality project results

  • Develop Clinical Department SOPs and participate in audits as needed

  • This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job. 

  • Employee must provide records of current training or complete training relating to HIPAA/PHI privacy, Human Subjects Protection, and GCP training.

  • Must maintain a current status on Natera training requirements including General Policies and Procedure Compliance and security training.

  • Employee must pass post offer criminal background check    

QUALIFICATIONS:

  • Bachelor's degree in life sciences, or other relevant discipline required, Advanced degree preferred.

  • 8 years of clinical research experience, including at least 4 years of experience in managing clinical trials as a leading role.

  • 4-7 years of experience in supporting clinical trials in a regulated environment .

  • Experience in managing CROs is preferred.

KNOWLEDGE, SKILLS, AND ABILITIES:

  • Knowledge and understanding of Clinical Trial SOPs, FDA Regulations, and ICH-GCPs governing the conduct of clinical trials

  • Demonstrated analytical skills and ability to identify problems and solutions independently

  • Ability to collaborate with the study team, cross functional team members and external collaborators

  • Proficiency in MS Word, Excel and PowerPoint

  • Good organization and planning skills

  • Strong interpersonal skills and communication skills (both written and oral)

  • Strong leadership skills, self-motivated, adaptable to a dynamic and fast paced environment

  • Must have excellent organizational and time management skills.

  • Ability to prioritize and handle multiple tasks and projects in a fast-paced environment

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