Be an early applicantLess than 25 applicants

Company

ProPharma · 5 hours ago

Central Study Coordinator

Raleigh, NC

Full-time

Remote

Entry Level

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BiopharmaMedical

H1B Sponsor Likely

Hiring Manager

Jed Huff

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Responsibilities

Responsible for clinical monitoring for assigned protocols and investigational sites

Ensuring that studies are conducted and documented in accordance with the study protocol

Standard operating procedures

Good Clinical Practices (GCP) and other applicable regulatory requirements

Qualification

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Technology managementResearch experienceWeb-based research platformsStudy Team experience

Required

Ability to manage technology and web-based research platforms on PC (Microsoft OS) laptop in the remote workspace

Critical thinking skills

Strong communication Skills (verbal and written)

Ability to work independently, and collaboratively with RAs/CSCs to complete delegated tasks as needed

Working location that has the ability to maintain privacy

Preferred

Research experience preferred

Study Team experience is ideal

Company

ProPharma

Glassdoor

3.1

ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies.

Founded in 2001

Overland Park, Kansas, USA

5001-10000 employees

http://www.propharmagroup.com/

H1B Sponsorship

ProPharma has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Trends of Total Sponsorships

2023 (4)

2022 (4)