Sr. Clinical Research Associate

Title: Seeking a Sr. Clinical Research Associate for Exciting Remote Opportunity on the East Coast

Introductory Paragraph:
Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) to join their team remotely on the East Coast. As a CRA with this innovative and growing organization, you will play a critical role in ensuring clinical trials are conducted ethically while adhering to regulatory guidelines.

Qualifications:
- Bachelor's degree in Life Sciences or related field
- Minimum of 5 years' experience with clinical site monitoring
- 1 year of ophthalmology experience
- Experience working within FDA regulations
- Experience working with a Sponsor company

Responsibilities:

1. Monitor Trials - Ensure that all protocols follow established policies & procedures through monitoring visits. 50% travel across the East Coast (expenses paid for)
2. Site Management - Develop strong relationships with study site personnel and provide guidance throughout entire process from start-up through close-out visit.
3.Clinical Data Review - Perform review data listings generated by CROs or internal data management staff against case report forms (CRFs).
4.Reporting - Prepare written reports including summarizing findings at Investigator Meetings.

Skills:
The following skills would be beneficial but not essential.
-Good communication abilities both verbal and non-verbal
-Knowledgeable about CTMS systems such as Medidata Rave

Rate:
$85-$100+ / hour

If you have significant experience conducting complex studies for pharma companies under your belt, then we urge you apply today!

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.