Welcome to a new career path with Rose Research Center!
Ready to be a Clinical Research Assistant for our company?
Who are we?
Rose Research Center (RRC) is a private research company specializing in nicotine and tobacco research. In the field of nicotine, smoking cessation, and harm reduction research we pride ourselves on being some of the best in the industry. Our leadership team brings over 100 years of industry-leading experience from their respective careers. Our CEO, Dr. Jed Rose, is recognized internationally for his contributions to this space including, but not limited to, the co-invention of the nicotine skin patch, inspiring the development of Chantix, among countless others.
What do we do?
We research new methods to save lives. RRC is a leader in the field of nicotine research. We work with the National Institutes of Health, Pharmaceutical partners, Industry partners, small businesses, non-profit organizations, and others to find an end to addiction to combustible nicotine products.
What we would like you to do.
RRC is seeking a Part-time Clinical Research Assistant to help conduct daily on-site and remote visit procedures in accordance with established protocols. RRC corporate office is in Raleigh, NC, North Carolina with an additional satellite office in Charlotte, North Carolina. This position will be based in Charlotte, NC.
The primary responsibility of this position is to interface with study participants. This will include study consenting, data collection, specimen collection, and implementation of study-related activities as outlined in study protocols and according to RRC’s Standard Operating Procedures (SOPs). The position involves seeing and working with study participants on a regular basis. Potential candidates should be detail-oriented, have a working knowledge of medical and research terminology, and be comfortable with various technology platforms. Candidates will need to possess strong multi-tasking skills in a fast-paced setting and can work both independently and collaboratively.
In this position, you will:
- Support Physicians, Research managers, and Clinical Study Staff with study-specific administrative tasks.
- Consent potential participants in clinical trials at RRC.
- Provide protection of sensitive health information, study data, and proprietary information.
- Collect pertinent visit assessment details ensuring the accuracy of all records connected with each research participant.
- Obtain vital signs and electrocardiograms.
- Obtain, process, and ship laboratory specimens onsite and to central laboratories.
- Provide professional input regarding participant visits both remote and on-site, assessments, evaluations, and determination of eligibility for study participation.
- Assist with transcription/data entry and review of completed Source Documents and Case Report Forms (CRFs).
- Complete all source documents, Case Report Forms (CRFs), and data entry into research management systems accurately and timely to assure compliance with study sponsors.
- Help participants to troubleshoot application issues and report problems.
- Respond to queries generated in Electronic Data Capture (EDC) systems.
- Ensure compliance with study protocols and RRC’s SOPs.
- Coordinate pick-up of outgoing packages with appropriate vendors.
- Prepare visit documents and ancillary supplies required for upcoming visits.
- Provide input during team discussions and meetings.
- Organize and assist with the maintenance of study logs.
- Organize incoming emails and participant binders.
- Assist with temperature-controlled study products.
- File study-specific documents daily.
- Work to create a positive work culture within RRC.
- Perform other related duties incidental to the work described herein.
Must have skills
- Excellent written, listening, and oral communication skills
- Good computer skills (MS Office products, spreadsheets, internet searches, e-mail)
- Familiarization with “smartphones”
- High attention to detail and accuracy
- Critical thinking skills for timely and effective problem-solving
- Excellent planning, prioritization, and organizational skills
- Excellent problem-solving skills
- Have and/or willing to obtain blood samples and phlebotomy certification
- Flexible work hours, if needed
- Works effectively on cross-functional teams
- Works well with individuals, participants, and/or patients
Company Benefits
- 401(k) Company matching
- Holiday, vacation, personal, and sick paid time off
Please submit your application to [email protected]
Job Type: Part-time
Pay: $18.25 - $21.00 per hour
Benefits:
- 401(k)
- 401(k) matching
- Paid time off
Education:
Ability to Commute:
- Charlotte, NC 28262 (Required)
Work Location: In person
