Associate Clinical Research Specialist Jobs in Missouri

A minimum of one (1) year experience in site oversight and management.

Expertise in oversight and managementvendors.

Company offers a great benefit package and competitive salary.

Assist the Study Lead carry out the responsibilities necessary to meet the constraints for the study.

Support clinical finance and the study's lead in evaluating, tracking, and directing study-specific budgets.

Three (3) or more years of experience in Clinical Research.

REMOTE Clinical Research Specialist ( Medical Device)- 6 months contract- May go perm

o Preferred, experience with electronic file system, Medidata and Sharepoint & Smartsheet.

5 + years, BA required. o Working as CRA (clinical research associate.)

o Familiar GDP (good documentation practices)

o Filling clinical trial documents ETMF

Administer Clinical research projects; collect investigator documentation, site management, clinical contact, and prepare monthly status reports.

Perform other duties as assigned by management.

BS/BA in appropriate field (e.g. Life Sciences, Pharmacy, or Nursing) or applicable education with relevant experience.

Independently manage sites confirming clinical study site operations are completed under site procedures

Experienced with numerous EDC systems

Experience in the pharmaceutical industry or hospital setting is preferable.

Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.

A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential

Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.

Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

You will be educated to degree level in a life science discipline or be a licensed healthcare professional.