Senior Clinical Trial Assistant
By Theery At Redwood City, CA, United States
Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
Maintain and manage requests for access to and deactivation of study systems users.
Competency of the drug development process with knowledge of ICH-GCP is a plus
Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
Distribute safety alerts and relevant documents, if required
Maintain and update study team and vendor contact information
Clinical Trial Monitor Jobs
By Medasource At United States
Monitor clinical trial progress through a combination of remote data review and on site monitoring visits. Some travel will be required.
3+ years of progressively responsible clinical trials experience with 2+ years of monitoring experience.
Assist in the development and writing of clinical trial monitoring plans.
Provide recommendations and guidance to study specific monitoring teams and assist in audit readiness and preparation.
Participate in regular monitoring team group meetings.
Bachelor's degree in a field relevant to research compliance
Clinical Trial Budget Negotiation Analyst - Remote
By UC San Diego Health At , San Diego $75,000 - $95,000 a year
Seven (7) years of related experience, education/training, OR a Bachelor’s degree in related area plus three (3) years of related experience/training.
Thorough knowledge of finance policies, practices, and systems.
Thorough knowledge and understanding of internal control practices and their impact on protecting University resources.
Demonstrated experience analyzing and drafting complex clinical trial budgets and negotiating mutually satisfying terms and conditions.
#122969 Clinical Trial Budget Negotiation Analyst - Remote
Candidates hired into this position may have the ability to work remotely.
Clinical Trial Nurse - Nyc, Ny
By IQVIA At , New York $67,000 - $83,200 a year
2+ years of peds experience
Recent experience in drawing blood
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Collecting samples and required information and data
IP preparation, administration, and post observation (1 hour)
Labelling and shipment of samples
Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Assistant Jobs
By RemeGen Biosciences At Pennsylvania, United States
Assist with general response to patient enrollment inquiries and seek management support when needed.
Manage SVP and study team calendars and set up meetings.
Excellent written and verbal communication skills.
Strong attention to detail and problem-solving skills.
· 3+ years of experience in health care, biopharmaceutical experience is strongly preferred.
Assist the clinical development teams in completion of all required tasks to meet departmental and project goals.
Director, Clinical Trial Recruitment
By Spectrum Science - a GHMC Company At New York City Metropolitan Area, United States
Meets deadlines, manages priorities and effectively communicates to team members, vendor partners and supervisors.
At least 5-7 years of clinical trial patient recruitment and retention experience working in a global clinical trial environment
Advanced knowledge of Microsoft Office (Outlook, PowerPoint, Word, etc.)
Excellent written and verbal communication skills; strong presentation skills
If you choose to go into an office, take advantage of the pre-tax transportation benefits.
If you choose to work from home, use the office equipment stipend.
Clinical Trial Intern - Dallas, Tx
By Medpace, Inc. At , Irving, 75038, Tx
Excellent organizational, communication, and prioritization skills;
Knowledge of Microsoft Office; and
Competitive compensation and benefits package
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Provide day-to-day project support activities - maintenance of project-related files, corresponding with study teams, etc;
Perform administrative duties in conformity with company policies and procedures;
Clinical Trial Research Assistant
By Durham Technical Community College At , , Nc $48,000 a year

% High School diploma or equivalent

Clinical Trial Coordinator (Cqm) - Home-Based
By ICON At , Remote
B.S. or Advanced Degree (or equivalent degree/experience in the opinion of the Hiring Manager)
Manages the collection and retention of training signature logs
Minimum of 1-4 years of relevant work experience
Strong communication (written and verbal) skills to be able to interact with internal Vertex groups as well as external groups
Demonstrates a working knowledge of ICH GCP regulations and clinical protocols
Distributes SUSAR reports to investigators
Clinical Trial Analyst Jobs
By Randstad Life Sciences US At Cambridge, MA, United States
Supporting additional ad-hoc activities as needed, as agreed with CTA Manager.
Maintaining knowledge of systems and processes.
Perform departmental tasks as needed.
Review and/or approval of study documentation, including essential document packets, study plans, informed consent forms, etc.
Supporting oversight of risk-based monitoring.
Attendance of key team meetings as required; may make presentations (e.g. data, etc.).
Associate Director, Clinical Trial Diversity Operations Lead
By GSK At Collegeville, PA, United States
Manage project budgets and track progress.
Experience working directly with physicians & patients to gather insights and understand their perspectives.
Leadership experience in a matrix environment with key internal and external stakeholders & partners.
Experience with US-based & Global-based Marketing programs.
Demonstrated ability to manage multiple projects simultaneously.
Excellent communication and interpersonal skills.
Clinical Trial Assistant / Etmf (Electronic Trial Master File) Coordinator
By Krystal Biotech, Inc. At Pittsburgh, PA, United States
Knowledge of clinical research processes, regulatory requirements, and good clinical practice (GCP).
Familiarity with eTMF systems and other clinical trial management systems.
Liaise with project managers, clinical operations staff, and other relevant team members to facilitate document collection and retention.
Monitor the progress of clinical trials and report updates to the project manager or clinical team lead.
Previous experience in a similar role, preferably within a pharmaceutical or biotech environment.
Excellent organizational skills and attention to detail.
Clinical Trial Monitoring Specialist
By Infosoft, Inc. At United States
3-5 years of experience required
Experience with medical device monitoring is required.
Experience with cardiac trials and/or blinded trials is preferred.
Experience with Medidata RAVE and Medidata CTMS is preferred.
Remote with frequent travel to clinical sites (Pacific or Mountain Time Zone)
remote and onsite monitoring activities
Clinical Trial Liaison Jobs
By Mirum Pharmaceuticals, Inc. At United States
Clinical site management experience, with an understanding of the operational aspects of clinical research and clinical development outsourcing
Excellent written and verbal communication skills - able to interact with all levels of internal and external management
Self-motivated with proactive issue monitoring and management including risk assessment and contingency planning
Other tactical or strategic requirements in line with the study team
5 years’ experience in clinical research in Pharma, Biotech or CRO or related experience
Demonstrated experience of working directly with clinical sites and investigators
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
By EG Life Sciences At United States
5+ years of Global Pharmaceutical Clinical Study Management:
1) 10+ years of Clinical Research Experience:
Audit & Inspection Readiness Experience:
ADDITIONAL QUALIFICATIONS / NICE TO HAVES
1) GCP and Clinical Quality experience
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
Clinical Trial Educator Jobs
By Actalent At Westerville, OH, United States

Description The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. The ...

Clinical Trial Educator Jobs
By Actalent At West Palm Beach, FL, United States

Description The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. The ...

Comparator Sourcing Specialist - Clinical Trial Supply
By Eurofins Lancaster Laboratories At Horsham, PA, United States
Good organizational and time management skills
Proven work experience, preferably in a GMP area
Proficiency in Microsoft Word, and experience with ERP preferable
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Acting as primary point of contact internally for comparator sourcing
Advises on appropriate sourcing strategy
Clinical Trial Assistant - Milan
By DOCS At All, MO, United States

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, ...