Clinical study protocols jobs

Clinical Research Coordinator II - Obstetrics and Gynecology

Washington University in St. Louis · Posted Nov 6, 2026

Open

Saint Louis, Missouri, United States
On-site
Full-time · Associate
$55K–$82K per year

Clinical Research Coordinator II - Obstetrics and Gynecology

Washington University in St. Louis · Posted Nov 6, 2026

Open

Saint Louis, Missouri, United States
On-site
Full-time · Associate
$55K–$82K per year

Clinical Research Coordinator II - Neurosurgery

Washington University in St. Louis · Posted Nov 4, 2026

Open

St. Louis, MO, United States
On-site
Full-time · Associate
$55K–$82K per year
2+ years

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Support the operations of a cerebrovascular biospecimen bank and associated clinical research program through specimen collection, patient engagement, and data management.

Compensation

Salary Range: $54,600.00 - $81,900.00 / Annually

Responsibilities

Identify eligible patients for enrollment in the cerebrovascular biospecimen bank using established screening criteria
Obtain informed consent from patients and/or their authorized representatives in accordance with IRB protocols
Collect samples from vascular surgical cases in coordination with the operative team
Perform blood and fluid draws at defined study time points
Process, label, and store biological specimens according to standard operating procedures to ensure sample integrity

Requirements

Bachelor’s degree

Skills

Clinical Research Clinical Study Protocols Database Management Research Projects Spreadsheet Analysis

Sr Medical Writer

Syneos Health · Posted Nov 4, 2026

Open

Remote, United Kingdom
Remote
Senior
3–5 years

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Lead the clear and accurate completion of medical writing deliverables for sponsor-dedicated projects across multiple countries.

Responsibilities

Leads the clear and accurate completion of medical writing deliverables
Manages medical writing activities associated with individual studies
Coordinates medical writing activities within and across departments
Leads the resolution of comments from the client
Completes a variety of documents including clinical study protocols, reports, patient narratives, annual reports, investigator brochures, informed consents, plain language summaries, periodic safety update reports, clinical development plans, IND submissions, integrated summary reports, NDA and eCTD submissions, journal manuscripts, abstracts, posters, and presentations

Skills

FDA regulations ICH regulations Good publication practices Medical writing Clinical study protocols Clinical study reports

Clinical Research Coordinator II - Obstetrics and Gynecology

Clinical Research Coordinator II - Obstetrics and Gynecology

Compensation

Responsibilities

Requirements

Skills

Benefits

Clinical Research Coordinator II - Neurosurgery

Compensation

Responsibilities

Requirements

Skills

Sr Medical Writer

Responsibilities

Skills

Benefits