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Clinical Cra Line Manager Jobs (NOW HIRING)

BeiGene USA

Associate Clinical Research Manager

$105K - $140K/yr

... CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain quality across clinical trials. As a line manager, this role leads a team to achieve ...

Penumbra

Clinical Research Associate II (Field CRA)

$89K - $130K/yr

General Summary The CRA II assists in the execution of clinical studies sponsored by Penumbra to ... Draft informed consents with supervision from line manager. * Assist with the development and/or ...

BeiGene USA

Senior Clinical Research Manager

... CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain quality across clinical trials. As a line manager, this role leads a team to achieve ...

Alira Health

Clinical Research Associate CRA

The CRA works closely with Lead CRAs, Sr CRAs, in-house CRAs, Associate Director of Clinical Monitoring and Project Managers to ensure protocol compliance, address site questions, and assist with ...

IceCure Medical

What You Will Do as a Clinical Research Associate (CRA) Clinical Study Execution & Site Management * Coordinate clinical study activities throughout the study lifecycle, from site selection and ...

Syneos Health Belgium BV

WI · On-site

Clinical Research Associate (CRA) - Belgique / België Syneos Health ® is a leading fully ... line management; technical and therapeutic area training; peer recognition and total rewards ...

New

BeiGene, Inc.

Associate Clinical Research Manager

$105K - $140K/yr

... CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain quality across clinical trials. As a line manager, this role leads a team to achieve ...

BeiGene, Inc.

Senior Clinical Research Manager

... CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain quality across clinical trials. As a line manager, this role leads a team to achieve ...

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Clinical Cra Line Manager information

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How much do clinical cra line manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for clinical cra line manager in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Clinical Cra Line Manager jobs?

For Clinical Cra Line Manager jobs, the most frequently searched job titles are:

Clinical Research Associate

Denver, CO • Remote

Tigermed America
See more jobs at Tigermed Americaexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago

Job description

1. Job Purpose:

  • This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations;
  • The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

2. Responsibilities:

  • Planning of project activities and study timelines based on project goal and sponsor's expectation;
  • Organize and Lead meeting/teleconferences for study activities implementation (e.g. investigator meeting, project review meeting etc), monitoring the progress of each CRA responsible sites, and assessing overall status of the project;
  • Develop the project management plan, monitoring plan etc as required for the study;
  • Develop study specific tools/forms, study templates as required for the study;
  • Develop and manage project budget;
  • Order and ensure all clinical supplies (including drug and non-drug) are adequate for all sites throughout the study period;
  • Ensure all team members have timely access to appropriate systems and tools, if applicable (e.g. IVRS, eCRF etc);
  • Organize and conduct site feasibility visits according to guidelines and make recommendation for final approval;
  • Track study progress and ensure project is conducted according to the plan;
  • Communicate to monitors new study information, study timelines and goals, study requirements. Responsible for raising overall project specific issues to management (e.g. Project Director, Senior Management);
  • Submit the weekly project report to management (e.g. Project Director, Senior Management);
  • Study site selection, initiation (SIV) and clinical monitoring;
  • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience;
  • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations;
  • Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol, and requirements;
  • Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files;
  • Finalize budget and obtain signed contract from site, prior to site initiation visit;
  • Provide guidance and training to entry-level CRA/CRA I/CRA II in collaboration with Line Manager.

3. Qualifications:

  • Bachelor degree or above in Medical, Pharmacology or Biology related major;
  • Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;
  • At least 1-3 years of Oncology CRA experience;
  • Good command of written and verbal English;
  • Good skills on Microsoft Word, Excel, PPT and Outlook, etc.;
  • Other abilities such as Communication skills/Information-gathering skills. Knowledge and/or experience in medical practice is a plus.

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