everyone deserves an opportunity to help advance medicine
- for themselves and for those they love. We are committed to connecting real-world opportunities in clinical research studies with people across the globe.
We educate and empower our patients who are partners in this work.
We are building the world's most passionate and skilled team of clinical researchers, and administrative team members, who are valued and supported over an entire career.
We create value for our sponsors worldwide by providing great service and timely, accurate results.
What makes us different?
Unlike our competitors, we are building a true platform, enabling team members, patients and partners to have the highest quality and consistent experience. We are effective across a broad range of therapeutic areas including Phase 1, oncology, and gene trials. We are intentional about our growth - choosing to grow where it benefits our patient diversity, capabilities, and research experience.
Our mission?
To connect people with the future of medicine through groundbreaking research, all while keeping the human experience at the heart of what we do.
How We Work
We are passionate about the work we do and strive to incorporate our Core Values in all we do. Our Core Values are:
Quality
Care
Be the Change You Seek
One Team
Grow for Good
Own It
Position Summary
The Data Management Specialist (
DMS) performs a variety of administrative activities to support the Clinical Research Coordinators in the successful conduct of clinical studies. The DMS will gain knowledge of protocols and regulatory requirements in order to provide a wide variety of administrative and clerical support.
Essential Functions
Gain familiarity of protocols and case report forms
Perform accurate, complete, and timely data entry of case report forms (CRFs) & timely query resolution
Meet data entry and query timelines as identified by sponsor
Highlight any missing information and/or errors in source documents
Assist CRPs in responding to data management queries, monitor findings, and follow-up
Support continued QC in the creation and maintenance of source documents, highlighting edits needed
Stay in constant communication with CRC and CRA to stay up to date with any new study related information.
Obtain, process, copy, scan, and file documents, as required
Process signed results and file, as required
Timely communication (phone, email, TEAMS)
Abide by GCP, SOPs, company guidelines, and local healthcare privacy regulations
Perform other administrative tasks as required by CRPs and Research Management
Education & Experience
Minimum:
HS/GED
At least 2 years experience in an administrative role
Experience working with multiple teams in a collaborative environment
Preferred:
Previous experience in a health care environment.
Benefits
Comprehensive health benefits
401(k) with company match
Continued opportunities for growth & development; yearly education allowance
Flexible PTO
Opportunities to work with internationally renowned physicians
Ready to be part of something bigger than yourself? We are excited to review your resume and cover letter explaining why you would be a good fit for our unique and fun team.
Centricity Research is an equal opportunity employer. We are committed to inclusive, barrier-free recruitment and selection processes and work environments. If you are contacted for a job opportunity, please let us know of any accommodations needed to ensure you have access to a fair and equitable process. Any information received relating to accommodation will be kept confidential.
Centricity Research does not currently utilize Artificial Intelligence for screening or recruitment purposes.
We thank all candidates for their applications, however, only those candidates selected for an interview will be contacted.
EDUCATION/EXPERIENCE
Minimum:
Canada: College/University degree in a relevant field of science is required
US: HS/GED
At least 2 years experience in an administrative role
Experience working with multiple teams in a collaborative environment
Preferred:
Previous experience in a health care environment.
CORE COMPETENCIES/SKILLS
Prerequisite (Essential):
Excellent communication skills (verbal and written)
Excellent computer skills (MS Word, Excel and Outlook)
Attention to detail
Ability to manage time efficiently
Self-directed
Teamwork & Collaboration
Proficient level of clinical, interpretive and analytical skills with organizational skills for project planning Flexible & Adaptable
Strong knowledge of ICH GCP, FDA & HC Division 5 guidelines Foundation:* Conflict resolution
Receptive to feedback
Empowering & Developing others
Empathy Skills
Planning and organizing skills
Excellent problem-solving skills
Achievement oriented
Analytical ability
Initiative
Decision making Leadership:* Forward thinking
Innovative
Creative
Strategic thinking
Self confidence
Strong interpersonal skills
PHYSICAL DEMANDS
Physical demands include but not limited to prolonged sitting, light lifting, standing, reaching, walking, and bending.
Frequently required to complete work on the computer in a seated position
May be required to lift light boxes (10 - 20lbs)
WORKING CONDITIONS
Modern medical office environment.
Required to follow all healthcare industry OHSA and OSHA guidelines
Required to perform duties in relation to PHIPA, HIPAA, PIDEDA
Some positions may require overnight/weekend hours
BENEFITS
Opportunities to work with internationally renowned physicians
Comprehensive health benefits, competitive salary
RRSP and 401(k) contribution matching
Continued opportunities for growth & development; yearly education allowance
* Paid holiday closures and employee appreciation days off
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