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Clinical Trial Researcher Jobs

Clinical Trial Supply Chain Specialist
By Mindlance At United States
SAP software based computer systems experience.
MS Office and MS Teams experience.
SKYPE Meeting or Virtual Meeting software experience.
GMP and Pharmaceutical Industry Regulations knowledge.
Ability to learn multiple computer systems.
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
Trial Clerk Jobs
By USAJOBS At Washington, DC, United States
Special Rating Factors (Knowledge, Skills, and Abilities Required by the Position):
Those who are required must abide by Selective Service registration requirements.
Trial Clerks Are Responsible For Providing Judicial Support Including
Taking notes of proceedings, notices, and rulings to prepare Court orders and minutes.
Responding to procedural questions from litigants, pro bono counsel, and the public.
Working closely with the Court's Docket Section to process exhibits, minutes, transcripts, orders, decisions, and other official case documents.
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 ...

Clinical Trial Educator - Remote | Wfh
By Get It Recruit - Educational Services At New Orleans, LA, United States

We are a leading healthcare organization dedicated to transforming lives through groundbreaking research and innovation.You will play a crucial role in driving trial recruitment, supporting ...

Clinical Trial Manager Jobs
By Invivyd At Waltham, MA, United States
Coordinate and lead study team meetings and update Clinical Operations management on timelines and progress toward milestones.
Participate in selection and management / oversight of external vendors; develop vendor specifications; review vendor reports, budgets and forecasts, and metrics.
Independent study management of phase 1 and 2 studies at sponsor company or a CRO
Strong oral and written communication skills
Ability to work remotely and independently under general direction in a fast-paced and dynamic environment
Coordinate activities and provide oversight of vendors and investigators to ensure compliance with the study protocol and overall clinical objectives.
Remote Clinical Trial Project Coordinator
By Confidential At Durham, NC, United States
Coordinates a multitude of CTM tactical and project management activities throughout the clinical trial lifecycle including forecasting/planning.
Management/tracking of global drug shipments; and Investigational Medicinal Product (IMP) accountability/ disposition.
NOTE: Can be fully remote but must be willing to come onsite the first 2 weeks for training.
Contract position: 1 year to start with potential for extension or conversion.
Note: 30-40 hours per week.
Implementation/oversight of IVRS/IWRS systems for drug supply.
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, ...

Clinical Trial Project Manager
By SRG At United States
3 years of relevant clinical research and project management experience with a CRO, pharmaceutical, biotechnology / device company
Strong project management skills including client management, fiscal / contract management, and quality management
Perform contract and financial management activities for assigned trials and serve as central point of contact with sponsor for project updates
Oversee all aspects of clinical research projects to assure applicable regulations, standard operating procedures, and sponsor requirements are met.
Bachelor’s Degree or equivalent experience
Good knowledge of FDA guidelines and review processes, IND and NDA processes, and GCPs
Clinical Trial Coordinator - Monitoring (Remote)
By Merck At United States
Effective time management, organizational and interpersonal skills, conflict management
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request, in collaboration with other country roles (if applicable)
Ensure proper provisioning for Learning Management System (CLMS) for all study site staff.
Credit Management within Learning Management System
Excellent negotiation skills for CTCs in finance area
Clinical Trial Assistant Jobs
By Precirix At Greater Boston, United States
·Expected educational qualifications: BSc or equivalent
·Minimum 2 years’ experience in with a clinical trial related role
·Experience with digital clinical trial systems such as eTMF, EDC, IRT etc
·Excellent communication skills (verbal, written and interpersonal) and negotiation skills
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Clinical Trial Manager Jobs
By Precirix At Greater Boston, United States
CRO oversight and study management
·Oversight of CRO including revieing monitoring reports, data management metrics, conducting oversight or co-monitoring visit etc.
·Expected educational qualifications: MSc or BSc
·Experience with digital clinical trial systems such as eTMF, EDC, IRT etc
·Knowledge within (radio/bio) pharmaceuticals and/or oncology will be considered as an advantage
·Excellent communication skills (verbal, written and interpersonal) and negotiation skills
Clinical Trial Manager Jobs
By Advanced Recruiting Partners At United States
· Maintains compliance in assigned region or project for performance, deliverables, and associated KPI’s.
· Ensures alignment of clinical activities to budget, including identification of out of scope activities.
· May participate in business development proposals, defense meetings and proposal development.
Clinical Trial Manager - Remote
By Actalent At New Hampshire, United States
1 - 3 years’ clinical operations / management experience from sponsor
Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills
Manages outsourced clinical operations functions, which may include contracted investigational supply, data management biostatistics, etc.
Ensuring that study Trial Master File is maintained and up to date and manages TMF audits as needed
Minimum BS/BA from an undergraduate program or equivalent experience
Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment
Clinical Trial Assistant, Langen Hybrid
By DOCS At All, MO, United States
If you have a completed education in any ad
medical device and government and public health
ife science area (hotel, business a
Clinical Trial Administrator-1 Jobs
By PharmiWeb.Jobs: Global Life Science Jobs At South Carolina, United States
Note - Specific skills and experience requirements may vary depending on the Country
Performs data entry into various databases/applications
Manages meetings/logistics, payments, and document archives
Undergraduate degree or relevant experience - at the discretion of the CRD
1 year experience in relevant administration (depending on the tasks required).
Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt
Clinical Trial Specialist Jobs
By Hawthorne Effect, Inc. At United States
Strong organization skills with experience with balancing priorities and resources.
Visit Management: Support logistics and visit scheduling teams by communicating relevant study information to Clinical Success team
Clinical Trial Experience is highly preferred but not required.
Strong skills in the use of technology, tools, operating systems, and software and is comfortable using these daily.
A creative and resourceful problem-solver with strong critical thinking skills.
GCP and good documentation practice expertise is required

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