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Clinical Trial Researcher Jobs

Remote - Senior Clinical Trial Specialist
By Beacon Hill Staffing Group At United States
5+ years previous clinical research experience in clinical trial coordination, site management, and or vendor management.
Must have the ability to build and maintain positive relationships with management and peers
Manage the collection, review and approval of regulatory documents from clinical sites
Manages and tracks study specific payments
Manage ancillary vendors, such as a specialty lab
Review site visit reports, under the direction of the Clinical Program Manager or designee
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 Nurse Navigator
By The Leukemia & Lymphoma Society At Rye Brook, NY, United States
Use problem solving skills to help patients overcome obstacles to enrollment
Maintain/increase knowledge and understanding of hematologic cancers, blood and bone marrow transplant and psychosocial aspects of living with cancer
Outstanding critical thinking, problem-solving, and collaboration skills
Demonstrated commitment to independent learning and skill enhancement
Serve in consulting role to the Information Resource Center about clinical trials
Contribute to continual process improvement of clinical trial support procedures
Regulatory Coordinator Iii/Clinical Researcher
By Cedars-Sinai At West Hollywood, CA, United States
Completes forms and generates all reports necessary to comply with regulatory requirements and institutional policies.
Establishes and maintains research files and documentation pertaining to regulatory requirements for clinical research/clinical trials.
May provide training and education to other personnel.
Participates in required training and education programs.
Five (5) years minimum of directly related experience; 2 years of regulatory experience and 3 years of clinical research experience.
Ability to identify areas of project interest and connect with appropriate support group: CCTO SPIN, IRB, Tech Transfer
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 Research Nurse I
By Kaiser Permanente At , San Francisco $148,200 - $191,730 a year
With supervision, assist in the accurate and appropriate study test article management.
Support the effective financial management of the clinical trial.
Other duties as assigned by appropriate management.
Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.
With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.
No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.
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.
Clinical Trial Coverage Analyst, Remote
By University of Maryland Medical System At Baltimore, MD, United States
Skill in cost/financial accounting and clinical trial management software.
IV. Knowledge, Skills, And Abilities
Bachelor’s degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting, Nursing, or a related field required.
Certification in Healthcare Research Compliance or Epic preferred.
Demonstrated skill tracking clinical and corporate contracts using electronic administration software such as Grant.gov, CICERO, OnCore, Epic, etc.
Creates coverage analysis grids and analyzes the performance of the actual coverage analysis.
Trial Attorney Jobs
By US Securities and Exchange Commission At , Los Angeles, 90071 $163,744 - $272,100 a year
If you are relying on your education to meet qualification requirements:
All qualification requirements must be met by the closing date of this announcement.
DRUG TESTING: This position may be subjected to drug testing requirements.
You will be evaluated for this job based on how well you meet the qualifications above.
CITIZENSHIP: This position is open to US Citizens.
You must possess a J.D. or LL.B Degree.
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.).
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
100% Remote- Clinical Trial Educator
By Actalent At Parsippany, NJ, United States
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Seeking 1 Clinical Trial Educator
PART TIME ROLE- 20hrs a week avg.
DE&I Are Embedded Into Our Culture Through

Are you looking for an exciting opportunity to make a real difference in the world of clinical research? We are seeking a Clinical Trial Researcher to join our team and help us develop innovative treatments for patients. As a Clinical Trial Researcher, you will be responsible for designing and executing clinical trials, analyzing data, and reporting results. You will have the opportunity to work with leading medical professionals and be part of a team that is making a real impact in the medical field. If you are passionate about clinical research and want to make a difference, this is the job for you!

Overview:

Clinical Trial Researchers are responsible for the design, implementation, and analysis of clinical trials. They work with medical professionals to ensure that the trials are conducted in accordance with the highest standards of safety and efficacy. They also collaborate with other researchers to ensure that the data collected is accurate and reliable.

Detailed Job Description:

Clinical Trial Researchers are responsible for designing, implementing, and analyzing clinical trials. They work with medical professionals to ensure that the trials are conducted in accordance with the highest standards of safety and efficacy. They also collaborate with other researchers to ensure that the data collected is accurate and reliable. They must be able to interpret and analyze the data collected from the trials and present their findings in a clear and concise manner. They must also be able to communicate effectively with medical professionals, other researchers, and sponsors of the trials.

What is Clinical Trial Researcher Job Skills Required?

• Knowledge of clinical trial design and implementation
• Knowledge of medical terminology and clinical trial protocols
• Ability to interpret and analyze data
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to work under pressure and meet deadlines
• Proficiency in Microsoft Office Suite

What is Clinical Trial Researcher Job Qualifications?

• Bachelor’s degree in a related field such as biology, chemistry, or public health
• Master’s degree in a related field such as clinical research, epidemiology, or biostatistics
• Certification in clinical research (CCRP)
• Experience in clinical research or related field

What is Clinical Trial Researcher Job Knowledge?

• Knowledge of clinical trial design and implementation
• Knowledge of medical terminology and clinical trial protocols
• Knowledge of data analysis and interpretation
• Knowledge of regulatory requirements for clinical trials

What is Clinical Trial Researcher Job Experience?

• Previous experience in clinical research or related field
• Experience in data analysis and interpretation
• Experience in clinical trial design and implementation

What is Clinical Trial Researcher Job Responsibilities?

• Design and implement clinical trials in accordance with the highest standards of safety and efficacy
• Collaborate with medical professionals and other researchers to ensure accuracy and reliability of data collected
• Interpret and analyze data collected from the trials
• Present findings in a clear and concise manner
• Communicate effectively with medical professionals, other researchers, and sponsors of the trials
• Ensure compliance with regulatory requirements for clinical trials