You haven't searched anything yet.
Overview
Lightship is the virtual-first provider that is perfecting the way clinical trials get done. Because clinical research plays such a vital role in bringing life-enhancing and lifesaving innovations to market, Lightship pursues operational excellence to clinical studies. Our end-to-end hybrid delivery model, our diversity of skillsets, and inhouse care team ensure sponsor success and the best possible patient experience. With a problem-solving mindset, we strive to make every clinical trial better than the last. Operational excellence is not a goal, but a way of doing things at Lightship.
This position is remote, and a successful candidate will possess a willingness and desire to work independently without significant oversight. Additionally, this position will require moderate travel.
We would like to offer you:
Generous benefits package, including:
ABOUT THE JOB:
In this role as a Clinical Study Coordinator, you will work in a pivotal role of coordinating communication and activities among patients, investigators, home health personnel, vendors, and other study personnel to prepare for and complete remote (via telemedicine) study visits, procedures, and assessments. You will assist the investigators, sub-investigators, and the Lightship team with the successful implementation and conduct of the research study while adhering to study protocol. You will understand and comply with all regulations, policies, and guidelines applicable to clinical research including GCP, FDA, and IRB requirements.
In this role as Clinical Study Coordinator, you will also collect study data, complete, and maintain source documents, and perform other day-to-day activities related to study conduct. You will work with various Lightship business units as needed to develop and implement standard research processes to successfully complete technology-enabled Direct-to-Patient (DtP) clinical research.
ABOUT THE IDEAL CANDIDATE:
We are looking for a strong communicator and effective problem solver with and exceptional ability to work as part of a team and to multitask effectively. You should have the ability to function independently and self-monitor the collected data per Good Documentation Practices. At least 2 years of related clinical or basic science research experience is required. You should ideally have a Bachelor’s Degree in Life Science or healthcare-related field. ACRP or CCRC certification or requisite combination of education, training, and experience is a plus. If you just so happen to also be bilingual in English & Spanish, that’s also a plus!
ABOUT THE APPLICATION PROCESS:
Are you the ideal candidate AND also willing to be very hands-on as we grow providing an exceptional and highly collaborative approach to clinical studies? Are you excited about the prospect to help re-envision how clinical research is executed with inclusivity, increased diversity, and accessibility at the core? If so, we invite you to Apply Now for immediate consideration for our Clinical Study Coordinator opportunity.
Our commitment to diversity & inclusion:
Lightship is an equal opportunity employer and promotes a diverse and inclusive workplace. Lightship considers all applicants without regard to race, color, religion, creed, national origin, age, sex, marital status, ancestry, disability, veteran status, gender identity, genetic information, sexual orientation, or any other status protected by applicable law. EEO is the Law
Lightship is an E-Verify employer. Find out more here: Right to Work Poster E-Verify Participation Poster
Please note: For the safety of our patients and each other, all positions at Lightship that require travel, in-person participation, or are patient-facing, do require vaccination against COVID-19.
#jobs #careers #nowhiring #hiringnow
Full Time
Durable Manufacturing
$54k-71k (estimate)
06/23/2022
03/27/2023
lightshipgroup.com
NORTH KINGSTOWN, RI
25 - 50
1998
THOMAS ALEXANDER
<$5M
Durable Manufacturing
The Lightship Group, LLC is a company based out of 606 Ten Rod Road, Wickford, Rhode Island, United States.
The job skills required for Clinical Study Coordinator (Contract) include Clinical Research, Clinical Trial, Problem Solving, Innovation, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Study Coordinator (Contract). That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Study Coordinator (Contract). Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Study Coordinator (Contract) positions, which can be used as a reference in future career path planning. As a Clinical Study Coordinator (Contract), it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Study Coordinator (Contract). You can explore the career advancement for a Clinical Study Coordinator (Contract) below and select your interested title to get hiring information.