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Associate Clinical Oncology Specialist Jobs

Oncology Clinical Data Specialist
By Northside Hospital Inc. At , Atlanta, 30342

support help support lung & esophageal case abstraction for the Society for Thoracic Surgery.

Clinical Care Associate, Inpatient Oncology
By Northside Hospital Inc. At , Atlanta, 30342

Overview: Northside Hospital is award-winning, state-of-the-art, and continually growing. Constantly expanding the quality and reach of our care to our patients and communities creates even more ...

Global Study Associate, Oncology R&D, Early Oncology Clinical
By AstraZeneca At , Gaithersburg, 20878, Md
Manage and contribute to the coordination and tracking of study materials and equipment.
Demonstrated verbal and written communication skills
Collect, review and track relevant study documents.
Assist in the tracking and reconciliation of invoices.
Support study team and provide study metrics / reports during the study, audits and regulatory inspections.
Liaise with internal and external participants and/or vendors. Track approvals and completion of required documents.
Clinical Trial Associate - Oncology
By BioSpace At New York, NY, United States
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
Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems
Excellent written and verbal communication skills, with the ability to effectively interact with study team members and internal / external stakeholders
Mental health and wellness benefits
Support the organization and conduct of investigator meetings, study initiation visits, and other trial-related meetings
Oncology Specialist - Rlt - Boston
By Novartis Oncology At Massachusetts, United States

Position is open due to an internal promotion. Preferred candidate has current Oncology sales experience in Boston.

Associate Clinical Oncology Specialist
By Natera At Orlando, FL, United States
Increase unit volumes by closing new physicians, accounts and growing volume in existing accounts.
Become product experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Work with assigned COS to sell, maintain & support existing customers
Travel to temporarily vacant geographies within an Area/Region to ensure continuity of customer support and business pull through.
Assess the needs of medical professionals and staff members with a focus on customer support, coordination of logistics, and problem solving
Promote quality client/patient relations and create a supportive climate by serving as a role model for other employees
Clinical Data Coordinator, Oncology
By ConcertAI At Greater Philadelphia, United States
Detect issues related to data capture, collection or management and suggest solutions.
Experience with medical records, clinical trial data entry into eCRFs, chart audit, or coding is required.
Provide subject matter expertise on clinical trial data entry into EDC systems utilized by sites and for leveraging on internal projects.
Use other resources as needed to gain the knowledge required to perform Clinical Data Coordinator work on new projects.
Share EDC eCRF and data query workflow knowledge and project-specific procedural knowledge with other Clinical Data Coordinators as needed.
Maintain a professional approach respecting the dignity and confidentiality of patients, associates, managers, and vendors.
Clinical Scientist (Oncology) Jobs
By Randstad Life Sciences US At United States
3+ years of industry-sponsored clinical trial management experience required.
Prior experience with clinical protocol development and/or regulatory submissions and management
Proactive stakeholder management and communication of progress and issues
Strong knowledge of clinical operations and the regulatory process - experience independently running/managing multiple clinical trials preferably within the oncology area
EDC including trial management, data review, issuing and resolving queries, CRF design/review/ approval
Additional post-graduate scientific experience or qualifications, such as an M.Sc. or PhD
Clinical Research Associate Ii, Oncology, East Coast Us Home-Based, Iqvia Biotech
By IQVIA At Durham, NC, United States
Effective time and financial management skills.
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Requires at least 1 year of on-site monitoring experience.
Good therapeutic and protocol knowledge as provided in company training.
Written and verbal communication skills including good command of English language.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Senior Clinical Research Associate (Oncology)
By Allucent At United States
Can demonstrate experience and knowledge in the CRO industry that will support POI’s management of clinical trials.
Assist the Project Team with the day-to-day management of clinical studies as required.
Monitoring Visit Report (MVR) review, management, resolution and escalation as required.
Relevant life science degree / medical / nursing background, or combination of education and experience.
Proven organizational abilities, and excellent written and oral communication and presentation skills.
A thorough knowledge of regulatory submission and reporting requirements and guidelines.
Associate Director, Marketing (Immuno-Oncology)
By AstraZeneca At Gaithersburg, MD, United States
Launch, management and customer facing experience
Experience building and integrating new capabilities that are relevant for brand success
Prior in-line HCP marketing experience
Oncology or specialty care experience highly preferred
In-depth Marketing experience (developing brand strategy, performing positioning, messaging, segmentation, targeting, leading ad agency, providing direction on annual budget planning)
Experience across multiple promotional channels (Personal, Non-Personal and Digital, Patient marketing)
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 Scientist I, Oncology Early Development
By BioSpace At North Chicago, IL, United States
Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
Provide/present key clinical study information to function/therapeutic area and management.
Experience in multi-faceted, broad-based multiple functions/therapeutic areas or clinical functions with in depth knowledge of clinical study issues.
Bachelors/Master’s degree, in Science related to Field with 11+ years’ experience in the pharmaceutical industry or Pharm-D/PhD with 1+years
Experience in team, drug development, and scientific project leadership or related.
Experience supporting clinical research, drug development and/or function/therapeutic area operations.
Clinical Care Associate, Ip Oncology
By Northside Hospital Inc. At , Atlanta, 30342, Ga

Overview: Northside Hospital is award-winning, state-of-the-art, and continually growing. Constantly expanding the quality and reach of our care to our patients and communities creates even more ...

Senior Clinical Research Associate (Phase I Oncology)
By Premier Research At , Remote
Perform remote monitoring activities for Phase I oncology clinical trials
Must have Oncology experience (Phase I preferred)
4+ years of independent on-site monitoring experience with all types of site visits
Identify and escalate potential risks and possible retraining opportunities for investigative sites.
Bachelor’s degree, or local equivalent, in a clinical, biological, scientific, or health-related field or its international equivalent
Completion of a CRA training program through a CRO
Clinical Document Management Associate (Tmf /Oncology) - 1 Year Contract – Hybrid- Nc Pharma
By Frankel Staffing Partners At Raleigh-Durham-Chapel Hill Area, United States
Support the management of eTMF documentation issues throughout the lifecycle of a study
Proactive management of clinical documentation and trackers
Experience working with documents at study start-up, during study conduct and close-out will be required
Experience in handling TMF documents during a regulatory inspection will be a plus.
Proactive and smart organizational skills
Excellent documentation skills and detail-orientation
Clinical Scientist, Oncology Early Development
By ABBVIE At , San Francisco, Ca
Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols
We offer a comprehensive package of benefits including paid time off. (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees
Collaborate cross-functionally to help create a scientific platform in support of the regulatory, commercial and medical education strategy for late-stage assets.
Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.
Responsible for providing focused scientific and clinical study support from start-up clinical study report (CSR).
Contribute to creation of electronic database, IRT, and associated training documents and review data completeness and fidelity throughout study conduct.
Associate Epidemiologist, Oncology Consultant
By Oracle At ,
Strong research background with experience conducting literature reviews.
Working knowledge of statistical analysis software tools (e.g., SAS, SPSS or STATA).
Experience with quantitative epidemiological and scientific analysis.
Medical or Pharmacy background or prior pharmaceutical industry experience a plus.
Excellent written and verbal communication skills.
Preference for candidates with up to 3 years’ related work experience.
Clinical Research Associate - Oncology
By DOCS At All, MO, United States
Experience conducting all types of MVs such as: Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site
l Medicinal Product, Local Study Managers and management team as appropriate.
Minimum 1 year of independent on-site monitoring experience
A demonstrated working knowledge of ICH/GCP Guidelines
Excellent record-keeping skills and attention to detail
You will be first to review "source to CRF/eCRF," ensuring patient safety and data integrity aspect of the study.
Associate Director, Commercial Analytics, Oncology
By Gilead Sciences At Foster City, CA, United States
Advanced analytics and people management skills
Management of projects, tasks, and activities of one or more direct reports (up to 1 - 2)
Management and relationship development with key stakeholder groups in Marketing and Commercial operations
Management of external consulting resources from a project delivery perspective
10 years of experience managing projects, initiatives, and people
Oncology pharma experience is highly desirable