-
Clinical Trial Associate
3 weeks ago
Accentuate Staffing Morrisville, United StatesAccentuate Staffing is partnering with a biopharmaceutical company who is hiring for a Clinical Trial Associate to join their team. This is a direct hire opportunity, offering competitive pay and benefits while working a hybrid work schedule. The ideal candidate has demonstrated ...
-
Associate Scientist
3 weeks ago
Actalent Durham, United States Full timeDescription: · Our client, a leading global clinical trial laboratory services organization providing focused on comprehensive testing, project management, supply chain, biorepository and specimen management, and clinical trial sample and consent tracking solutions is seeking Ass ...
-
Medpace Raleigh, United StatesJob Summary · Medpace is the leading CRO for Biotech companies and is continuing to add established Project Managers to join our Clinical Trial Management Group. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience ...
-
Associate Director, Clinical Trial Management
4 weeks ago
Medpace Raleigh, United StatesJob Summary · Medpace is the leading CRO for Biotech companies and is continuing to add established Project Managers to join our Clinical Trial Management Group. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience ...
-
Associate Director, Clinical Trial Management
2 weeks ago
Medpace Raleigh, United States Full timeMedpace is the leading CRO for Biotech companies and is continuing to add established Project Managers to join our Clinical Trial Management Group. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. We ...
-
Medical Monitor
1 week ago
IQVIA, Inc. Durham, United StatesJob Overview · The Medical Monitor is a responsible member of a clinical team dedicated to the development and execution of the clinical and operational implementation of clinical trials. The Medical Monitor provides active medical contribution to the cross-functional clinical te ...
-
Associate Director, Clinical Research
1 week ago
Shattuck Labs, Inc. Durham, United StatesAbout the position: · The Associate Director/Director of Clinical Research, in collaboration with the Medical Monitor, is responsible for the design, conduct, analysis, and reporting of clinical trials. This individual will assume a lead role in trial planning and execution, work ...
-
Duke University Durham, United States Full timeAt Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advance health together. · About Duke Health's Patient Revenue Man ...
-
Associate Director Clinical Compliance #3741
3 weeks ago
Grail Durham, United StatesGrail's Clinical Quality Assurance (CQA) department is seeking a compliance expert to support compliant conduct of Grail's clinical studies and to support Grail's partnerships with pharmaceutical companies for companion diagnostic (CDx) tests. · The Associate Director will work c ...
-
Clinical Research Associate II, DCRI
3 weeks ago
Duke University Durham, United StatesSchool of Medicine · Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clini ...
-
Clinical Trials Project Leader II, DCRI
3 weeks ago
Duke University Durham, United StatesSchool of Medicine · Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clini ...
-
Clinical Trial Manager
1 week ago
BioSpace Durham, United StatesJob Details · Summary · The Clinical Trial Manager (CTM) is responsible for the management of clinical trial(s) from vendor selection through Clinical Study Report (CSR) completion. The CTM is accountable for successful delivery of assigned clinical team activities at the project ...
-
Clinical Trial Manager
1 week ago
Precision Biosciences Durham, United StatesSummary · The Clinical Trial Manager (CTM) is responsible for the management of clinical trial(s) from vendor selection through Clinical Study Report (CSR) completion. The CTM is accountable for successful delivery of assigned clinical team activities at the project level by meet ...
-
United Therapeutics Durham, United StatesCalifornia, US residents click here ) . · **The job details are as follows:** · **What We Do** · We build on the strength of our research and development expertise and a distinctive, entrepreneurial culture that encourages diversity, innovation, creativity, sustainability, and, s ...
-
Clinical Trials Coordinator II, DCRI
1 week ago
Duke University Durham, United StatesSchool of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinici ...
-
Manager, Clinical Trials
3 weeks ago
Grifols Shared Services North America, Inc RTP, United StatesWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the worl ...
-
Clinical Research Coordinator
3 weeks ago
Duke University Durham, United StatesSchool of Medicine · Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clini ...
-
Duke University Durham, United States Full timeAt Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advance health together.About Duke Health's Patient Revenue Manage ...
-
Associate Director, Clinical Operations
3 weeks ago
Grifols Shared Services North America, Inc RTP, United StatesWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the worl ...
-
Associate Director, Clinical Research
1 week ago
Shattuck Labs, Inc. Durham, United StatesJob Description · Job Description · About the position: · The Associate Director/Director of Clinical Research, in collaboration with the Medical Monitor, is responsible for the design, conduct, analysis, and reporting of clinical trials. This individual will assume a lead role ...
Clinical Trial Associate - Durham, United States - Revolobio
Description
Job Title:
Clinical Trial Associate
Schedule:
Full-time
Location:
Durham, North Carolina
Reports to:
Director, Clinical Operations
Our Core Values:
All employees, including Executives, are expected to uphold REVOLO's Core Values.
These are the values we hold which form the foundation on which we interact and collaborate, perform our work, and conduct ourselves.
They are the guiding practices we are expected to use every day in everything we do.Revolutionary I Excellence I Respect I Integrity I Trust I Patient Well-being
Who We are:
If you're looking for a typical biotechnology company, you've come to the wrong place.
We are a revolutionary biotherapeutics company and our mission is to revolutionize autoimmune and allergic disease treatment by resetting the immune system for superior long-term disease remission.
How We Succeed:
By developing therapies that achieve superior long-term disease remission from less frequent chronic dosing and without suppression of the immune system.
Why
We Do What We Do:
Existing therapies for autoimmune and allergic diseases require frequent chronic dosing, provide only short-term disease remission in a limited number of patients and suppress the immune system, ultimately putting patients at risk of developing serious infections and life-threatening side effects.
How You'll Contribute:
The Clinical Trial Associate will work closely with clinical operations and help plan clinical trial execution with the expectation and vision to obtain the highest data quality in a manner compliant with quality standards, regulatory guidance and within budget.
This is a hands-on role that will assist with documenting and reporting the clinical development program, study sites, clinical trial vendors as well as the execution, and completion of clinical trials.
The position will work cross-functionally to ensure quality clinical operations execution.Responsibilities:
Support clinical study documentation preparation, tracking and maintenance.
Maintain trial master files (TMFs) and study documentation in accordance with regulatory requirements and internal SOPs.
Develop and maintain study-related trackers to support Clinical Operations
Assist in planning, organizing. and executing study-specific meetings. Write and distribute agendas. minutes. and regular updates.
Maintain and update the study team list. including vendor contact information.
Review and update system access user lists at pre-specified frequencies.
Participate in reviewing, formatting, and finalizing study-related templates, logs, plans, and manuals.
Support the monitoring and tracking of a study progress, including- patient recruitment and enrollment, to ensure adherence to study timelines and milestones.
May ;support financial tasks for the study (e.g. investigator/institution/vendors payments), coordinating tracking.Perform other duties in support of Clinical Operations, as required.
Other duties as assigned.
Position Requirements And Experience:
Bachelor's or advanced degree in a relevant scientific discipline (e.g., Life Sciences, Pharmacy, Nursing or Medicine).
Previous experience working as a Clinical Trials Associate Study Coordinator or in a similar role within the pharmaceutical, biotechnology, or CRO industry preferred.
2 or more years working within pharmaceutical, biotechnology, or CRO industry is preferred.Knowledge of clinical trial regulations, guidelines, and best practices, including ICH¬GCP and FDA requirements.
Strong organizational skills and attention to detail, with the ability to manage multiple tasks and prioritize workload effectively.
Excellent written and verbal communication skills with the ability to effectively interactwith study team members and internal and external stakeholders.
Ability to work independently as well as collaboratively in a team-oriented environment.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Project).
This position requires extended periods of sitting and working on a computer. Must have the ability to navigate travel both internationally and domestic.
Revolo Biotherapeutics is an Equal Opportunity/Affirmative Action Employer – EOE Minorities/ Females / Protected Veterans / Individuals with Disabilities.
#J-18808-Ljbffr
