Clinical Research Coordinator (Ophthalmology/Remote) – Niche CRO -Direct Hire

Our client, a niche CRO therapeutically focused on Ophthalmology trials, is actively recruiting for a very organized, capable and industrious candidate to assume a key support role on its Clinical Study Management team.  This Clinical Research Coordinator will provide broad-reaching support to internal study teams, sponsor clients and assigned clinical research sites.  We seek a go-getter who gets things done.

Experience working on Ophthalmology trials is a strong plus.

This position can be remote, located anywhere in the US and the Company will offer a generous salary and benefits (to include unlimited PTO, 40 hour work week max, great health benefits) to attract and retain a star.

Key Things to Note:

• This is an established niche CRO with therapeutic expertise in posterior and anterior segments of ophthalmology. 
• This Clinical Research Coordinator will be responsible for providing support to Study Management Teams. 
• This is a highly collaborative role involving regular interaction with clinical cross-functional team members and clients.  Experience supporting clinical teams in a clinical research setting will be important.

Duties will include:

• Tracking multiple aspects of the study and communicating information to the study team, escalating issues as appropriate.
• Providing administrative support for amendments, trackers, and follow-up with sites.
• Developing and providing reports to update study management and summarize study progress and status.
• Responsible for site support during study start-up, communicating with site staff regarding the collection and status of essential documents, study supplies, mass communications, enrollment survey follow-up, and other study related information and actions.
• Assisting study team in collection and tracking of essential documents, IRB submissions, procurement and shipment of supplies to sites.
• Assisting with review of both internal and external documents, including essential documents and IRB applications. 
• Maintaining clinical trial master files (TMF and eTMF) and keeps all documentation current.  Assists with inventory of the TMF/eTMF.
• Providing meeting agendas, minutes and action items for study related meetings.
• Coordinating study team activities on behalf of study management.

Targeted candidate will offer a BA/BS degree and 3+ years of clinical support experience in a Pharma, Biotech, CRO or Clinical Research Setting. 

Finally, we seek a motivated self-starter who can take initiative.  An independent, knowledgeable and flexible professional who will work exceedingly well in a dynamic and collaborative setting; One who can adapt to changing priorities and one who has the ability to take initiative to complete tasks under tight deadlines.

This is a direct hire role.  Please forward Word resume for prompt consideration.