Register
Recruit Create CV

Medical Advisor Clinical Trials Jobs

Clinical Advisor Jobs
By CAMRIS At Bethesda, MD, United States
Experience in the conduct and management of clinical trials, phase I - III vaccine or monoclonal antibody clinical trials preferred.
Serve as primary reviewer for pharmacy management plans, monitoring and audit reports.
CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at
Evaluate site Pharmacy Establishment Plans for the qualification to conduct clinical trials.
Identify the local requirements by national regulators in conducting multi-national clinical trials in study drug utilization.
Assess impact of local, regional, and global requirements and considerations on drug labeling and utilization.
Remote Clinical Trials Manager - 210641
By Medix™ At United States
Possess a minimum of 7 years of clinical trial management experience, with a focus on recent Oncology trials.
Train team members and partners, maintain study files, provide regular updates to management, and ensure compliance with GCP.
Lead study teams, foster relationships with external partners (CROs, labs, IRBs, sites), and identify/manage risks.
Assist in site selection, create RFPs, negotiate contracts, manage budgets, and oversee invoicing.
Show experience in international trials and managing external providers, including CROs.
Efficiently oversee clinical trials, managing multiple studies within a development program.
Clinical Trials Associate - Neuroscience
By Worldwide Clinical Trials At United States
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Skill sets and proven performance equivalent to the
Maintain and quality audit to assure the most recent revisions of documents are on project portals
Clinical Trials Manager/Sr Clinical Trials Manager
By Medix™ At Gaithersburg, MD, United States
At least 5 years of clinical trial management experience; Recent Oncology trial
Effective trial management of a clinical study or multiple studies within a clinical
Management of the study team for assigned studies or programs and of relationships with
Provide management with routine updates regarding the status of ongoing studies
Understanding of cross-functional areas including data management / biostatistics,
Brochures, Study Manuals, Statistical Analysis Plans, CRFs, Data Management Plans, and
Medical Advisor Jobs
By Intellectt Inc At United States
Strong multi-tasking and project management skills needed.
Strong marketing skills in the pharmacy clinical services space and/or marketing to pharmacists.
Strong communication skills with demonstrated ability to create and deliver
Lake Forest, IL - 60045 (remote role)
Demonstrated understanding of the varied payment models utilized at the sites of care for the ID testing portfolio.
Professional and impactful presentations to senior leaders.
Project Associate (Remote), Clinical Trials Office
By University of Virginia At National, MD, United States
Experience with the following computer applications: OnCore, EPIC, Advarra EDC, other clinical trial management systems and electronic data capture system.
Assist PI and CTO Project Managers in incorporating multi-site requirements/aspects into a developing protocol.
Supporting CTO Project Managers With Study Study Monitoring and Management:
Manage SAE/DLT information. Prepare and submit reports to the FDA, drug manufacturer and/ or participating sites, as applicable.
2-4 years of experience as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) and/or Research Project Associate.
Working knowledge of state and federal guidelines as they apply to the conduct of clinical research.
Clinical Trials Nurse – Sarcoma Outpatient Setting, Nyc
By Memorial Sloan Kettering Cancer Center At , New York, 10017 $87,300 - $139,800 a year
Perform patient assessment, offer patient education and patient/family support
Three years clinical Nursing experience
Clinical research nursing experience preferred but not necessary
Providers of compassionate, evidence-based nursing care to Oncology patients and families living with cancer in a healing and innovative environment
Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
A good decision-maker, with proven success at making timely decisions that maintain high standards of nursing care within the organization.
Project Associate (Remote), Clinical Trials Office
By The Rector & Visitors of the University of Virginia At , $65,000 - $75,000 a year
Assist PI and CTO Project Managers in incorporating multi-site requirements/aspects into a developing protocol.
Supporting CTO Project Managers With Study Study Monitoring and Management:
Manage SAE/DLT information. Prepare and submit reports to the FDA, drug manufacturer and/ or participating sites, as applicable.
2-4 years of experience as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) and/or Research Project Associate.
Working knowledge of state and federal guidelines as they apply to the conduct of clinical research.
Knowledge of GCPs governing clinical research.
Senior Project Manager, Rwe Clinical Trials, Remote
By WALGREENS At , Deerfield, 60015 $143,460 - $196,010 a year
Bachelor’s degree in Life Sciences or related field and at least 4 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (ie. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
May manage a team as and when required
Identify changes in scope and manage the change control process, as necessary
Project Manager, Rwe Clinical Trials (Remote)
By Walgreens At Deerfield, IL, United States
Bachelor’s degree in Life Sciences or related field and at least 2 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (i.e. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
Identify changes in scope and manage the change control process, as necessary
Experience collaborating with others to deliver results to meet timeline, metrics and budget.
Clinical Trials And Site Operations Manager
By Re:Cognition Health At Chicago, IL, United States
Operations Management: 2 years (Required)
The successful applicant will have access to all Re:Cognition Health’s benefits.
Chicago, IL 60611: Reliably commute or planning to relocate before starting work (Required)
Clinical Trials Coordinating: 3 years (Required)
Clinical research: 4 years (Required)
The post holder is responsible for:
Clinical Trials Associate - Cancer Institute
By Bayhealth At Dover, DE, United States
Evaluates patients’ progress toward attaining expected outcomes. Demonstrates the ability to reflect knowledge of current professional practice standards, laws and regulations.
All other duties as assigned within the scope and range of job responsibilities
Education Master Degree Master Degree Master Degree Science Health Care Related field
Credential Certified Clinical Research Associate
Business Development Manager, Clinical Trials
By Clinitiative Health Research At Dallas, TX, United States
Ensure client satisfaction through continued relationship management
1+ years of experience in the clinical research industry, or similar 
Salesforce experience is a plus
Experience with clinical trials is a plus
A self-starter and a hunter’s mentality 
Bachelor's of Science, is a plus 
Project Leadership – Biotech (Clinical Trials) – Vaccine - Home Based
By Parexel At Durham, NC, United States

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, your ...

Clinical Trials Associate - Early Phase
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Clinical Trials Associate- Oncology
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Clinical Trials Assistant I - Clinic
By Institute for Medical Research At Durham, NC, United States
Assist in the collection and management of clinical data and collection of source documents
Review CPRS (Computerized Patient Record System) patient charts to screen for possible subjects and to compile data
Perform tasks to ensure smooth clinic flow including organization of supplies, preparation of paperwork, and communication with study and clinical staff
Recruit and consent research participants for various clinical trials and research projects
Trouble-shoot and modify protocol implementation when necessary
Obtain various measurements from participants including vital signs and waist and hip circumference
Medical Writer Clinical Trials
By Hackensack Meridian Health At , Hackensack, 07601, Nj
Education, Knowledge, Skills and Abilities Required:
Education, Knowledge, Skills and Abilities Preferred:
Ensures potential study risks are escalated to management as appropriate.
Mandatory education on human subject research and GCP (CITI Training and Certification).
Excellent medical writing, communication, organizational, presentation, documentation, and interpersonal skills are required.
Possesses beginning to working knowledge of subject matter.
Clinical Trials Research Associate - Gastroenterology/Hepatology
By The University of Iowa At , Iowa City, Ia
Protocol Development/ Management and Study Responsibilities:
Excellent time management skills and the ability to perform detail oriented work independently is required
Experience with following specific protocol techniques and management is desirable.
Manage and organize regulatory documentation from sites and regulatory authorities.
Manage and organize regulatory documents from sponsors and CROs.
Excellent written and verbal communication skills are required.
Project Leadership - Clinical Trials -
By Parexel At , Remote

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, ...

Are you looking for an exciting opportunity to use your medical expertise to help shape the future of healthcare? Join us as a Medical Advisor Clinical Trials and help us develop innovative treatments that will improve the lives of patients around the world!

Overview Medical Advisor Clinical Trials is a specialized role within the medical field that focuses on the clinical trial process. This role is responsible for providing medical advice and guidance to clinical trial sponsors, investigators, and other stakeholders throughout the clinical trial process. The Medical Advisor Clinical Trials is responsible for ensuring that the clinical trial is conducted in accordance with applicable regulations and guidelines, and that the safety and efficacy of the trial are maintained. Detailed Job Description The Medical Advisor Clinical Trials is responsible for providing medical advice and guidance to clinical trial sponsors, investigators, and other stakeholders throughout the clinical trial process. This includes providing medical input into the design, implementation, and monitoring of clinical trials, as well as providing medical advice on the interpretation of clinical trial results. The Medical Advisor Clinical Trials is also responsible for ensuring that the clinical trial is conducted in accordance with applicable regulations and guidelines, and that the safety and efficacy of the trial are maintained. Job Skills Required
• Knowledge of clinical trial design and implementation
• Knowledge of applicable regulations and guidelines
• Ability to interpret clinical trial results
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
Job Qualifications
• Medical degree (MD, DO, or equivalent)
• Board certification in a relevant specialty
• Clinical research experience
• Previous experience in a medical advisory role
Job Knowledge
• Knowledge of clinical trial design and implementation
• Knowledge of applicable regulations and guidelines
• Knowledge of medical terminology and clinical trial terminology
• Knowledge of medical ethics and patient safety
• Knowledge of medical data analysis and interpretation
Job Experience
• Previous experience in a medical advisory role
• Previous experience in clinical research
Job Responsibilities
• Provide medical advice and guidance to clinical trial sponsors, investigators, and other stakeholders throughout the clinical trial process
• Ensure that the clinical trial is conducted in accordance with applicable regulations and guidelines
• Monitor the safety and efficacy of the trial
• Interpret clinical trial results
• Provide medical input into the design, implementation, and monitoring of clinical trials
• Prepare and review clinical trial documents
• Participate in meetings and conferences related to clinical trials