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Remote Clinical Study Start Up Jobs (NOW HIRING)

Alnylam Pharmaceuticals

Sr. Manager, Study Start Up

The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading ... Remote U.S. Pay Range $140,300.00 - $189,900.00 The pay range reflects the full-time base salary ...

BeiGene USA

Global Clinical Study Senior Manager

Study start-up strategy * Enrollment acceleration plans * Site activation timelines * Data flow and ... Clinical Operations (regional teams / RCSMs) * Medical, Regulatory, Biometrics, Supply, etc.

New

Emmes

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

BeiGene USA

Regional Clinical Study Senior Manager

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

... start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM IV) / Senior ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

Tempus

Study Start-Up Specialist

$55K - $70K/yr

... study start-up related questions ... Coordinate with TIME sites and sponsor teams to activate clinical trials through the JIT and ...

BeiGene USA

Regional Clinical Study Manager

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...

Medpace, Inc.

Study Start-Up Project Manager

Irving, TX · On-site +1

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...

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Remote Clinical Study Start Up information

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$22K

$125.3K

$206K

How much do remote clinical study start up jobs pay per year?

As of Sep 5, 2026, the average yearly pay for remote clinical study start up in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is the difference between Remote Clinical Study Start Up vs Remote Clinical Data Coordinator?

AspectRemote Clinical Study Start UpRemote Clinical Data Coordinator
Primary ResponsibilitiesPlanning, site selection, regulatory submissions, site initiationData entry, data validation, database management, data quality assurance
Required CredentialsLife sciences degree, knowledge of GCP, regulatory knowledgeLife sciences or related degree, familiarity with clinical data systems
Work EnvironmentCollaborates with sponsors, sites, regulatory bodiesWorks mainly with data management teams and databases
Industry UsageInvolved early in trial setup phasesInvolved during data collection and analysis phases

Remote Clinical Study Start Up focuses on preparing and initiating clinical trials, including site selection and regulatory compliance. In contrast, Remote Clinical Data Coordinator manages and ensures the accuracy of clinical trial data during the study. Both roles require related credentials and work within the clinical research industry, but they operate at different stages of the trial process.

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Remote Clinical Study Start Up jobs near you
Infographic showing various Remote Clinical Study Start Up job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 63% Full Time, 17% Part Time, and 19% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Study Start Up Lead Contractor

Entrada Therapeutics

Boston, MA • Remote

Part-time, Contractor

Posted 16 days ago

Job description

The Perfect Addition to Our Team

You are excited about the opportunity to spearhead clinical trial start up activities. You are well organized and like to share best practices in clinical operations and study start up. You enjoy a fast-paced environment and juggling competing priorities and are willing to jump in and help wherever it is needed. You follow up and follow through, efficiently connecting problems with solutions. You work successfully in a team environment and have strong interpersonal skills, in order to effectively build working relationships inside and outside of the company.

The Opportunity

This individual will partner with study leads on varying operational initiatives across on-going and new clinical studies for study start up and enrollment. This role will support the overall

planning and management of clinical trials, including CRO and vendor oversight, to achieve project milestones and clinical study timelines in alignment with company goals and in compliance with local, ICH, GCP, and company policies and procedures.

Responsibilities
  • Lead and/or support Sr. CTMs/CTMs with study start up and maintenance activities, including regulatory submissions, country and site selection, site budget management, site activation, ICF review, etc.
  • Collaborate with Sr. CTM/CTMs on developing study specific strategic start up or protocol amendment implementation plans.
  • Drive start-up activities including timely site selection and activation, EC submissions and query responses, document collection, and protocol amendment activities.
  • Reviewing country-level ICFs and related site or patient facing materials and routing for approval by required functional areas.
  • Review and approve site activation packages and regulatory documentation, ensuring complete and accurate information tracked in the appropriate databases.
  • Proactively identify and support resolution/escalation of issues impacting start up or trial execution.
  • Collaborate and communicate with the cross-functional trial team, including collaborating with internal team members and external vendors on related study start up activities.
  • Ensure that all assigned start up activities are on track and support study deliverables.
  • Partner with relevant stakeholders to develop and implement appropriate study-specific training and kick-off meetings to all relevant study-related personnel (internal, CRO, Site staff, and other relevant 3rd parties)
The Necessities

At Entrada, our passion for science, our devotion to patients and our values drives our behavior:

  • Humanity - We genuinely care about patients and about one another.
  • Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.
  • Creativity - We are creative problem solvers.
  • Collaboration - We are more than the sum of our parts.
  • Curiosity - We have a growth mindset and push conventional thought and theory.

To thrive on our team, you will need to come with:

  • BA/BS degree with 8 + years of combined experience supporting and independently managing clinical trial activities globally.
  • Strong knowledge of ICH/GCP and regulatory requirements.
  • Strong experience in the drug development process, including trial design, trial planning and management, and CRO and vendor oversight.
  • Excellent verbal and written communication skills.
  • Proven ability to work effectively across functions.
  • Ability to travel approximately 10% of the time, as determined by the needs of the business.

This is a part-time, long-term contract position estimated to be ~20-30 hours per week. The role is a US based remote position, with preference given to local New England based candidates. This role may require ad-hoc travel to the Entrada Therapeutics Headquarters located in Boston, MA. #LI-JF1 #LI-Remote 

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