External

👥 10-50 Business Intelligence Apps Software💼 Private Company

External is a dedicated team of clinicians, scientists, and researchers committed to enhancing healthcare through authentic, personalized attention. With a focus on adapting to the rapidly changing industry landscape, they cherish the diverse backgrounds and motivations of their members, which contribute to their unique approach.

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🔥 Vice President, Medical Affairs - Endocrinology - U.S. Remote

Posted 1 day ago

📍 United States of America

🧭 Full-Time

🔍 Clinical Research Organization (CRO)

Medical Doctor (MD) with 12 or more years of experience in clinical research and drug development.
Knowledge of operational aspects of Phase I-IV clinical research and experience in CROs or pharmaceutical companies.
Demonstrated ability to maintain effective relationships with clients, KOLs, and vendors.
Detail-oriented, able to work under pressure and tight timelines.
Ability to supervise and mentor direct reports.
Highly ethical and medically oriented.

Drive development of new business via the Business Development (BD) team, including initiation/retention of relationships with clients.
Participate in BD opportunities through presentations, proposal writing, and closing opportunities.
Build relationships with Key Opinion Leaders and therapeutic experts.
Support existing operational teams in maximizing sales and repeat business.
Increase Worldwide Clinical Trials brand awareness through publications.
Supervise and mentor medical staff, ensuring successful project execution.
Provide support in KOL and DSMB meetings, and represent medical affairs in corporate initiatives.
Implement Medical Monitoring initiatives and provide therapeutic training.

LeadershipProject Management

Posted 1 day ago

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🔥 Central Monitor REMOTE CANADA/MEXICO/BRAZIL

Posted 3 days ago

📍 Canada, Mexico, Brazil

🔍 Clinical Research

BSc/RN or equivalent combination of knowledge, skills, and experience.
At least 3 years' experience in clinical research required.
Prior experience in Central Monitoring and knowledge of ICH/Regulatory guidance is required.
Demonstrated critical thinking skills for identifying issues and solutions.
Capability of working in a global environment.
Excellent communication and time management skills.

Perform central monitoring activities including reviewing system outputs and identifying outliers.
Propose actions for the assessment by the study team and follow up as needed.
Document the centralized monitoring strategy and develop the central monitoring plan.
Conduct site-level reviews of Key Risk Indications/Key Performance Indicators.
Ensure inspection readiness for centralized monitoring scope.
Present at Central Monitor Forum meetings.

SQLData AnalysisExcel VBAAnalytical SkillsCritical thinking

Posted 3 days ago

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🔥 Senior Clinical Data Manager - UK - Remote

Posted 6 days ago

📍 United Kingdom

🔍 Clinical Research Organization (CRO)

Educated to degree level (preferably in Life Science), Nursing qualification, or relevant industry experience.
Experience in Data Management or related fields.
Strong computer literacy with willingness to adapt to various systems.
Attention to detail with ability to question data validity.
Ability to train new staff and monitor their performance.

Manage each of the data management projects to which assigned and provide leadership to the data management teams.
Represent WCT in dealings with Sponsors regarding the Data Management aspects of projects.
Liaise with the Director, Data Management to discuss project progress and issues.
Oversee staff training and monitor performance.
Ensure data management operations comply with WCT SOPs and contribute to their revision.
Create and review project-specific documentation for assigned trials.
Ensure adequate QC checks and Database Quality Assessments on clinical databases.

LeadershipSQLData AnalysisAttention to detailData management

Posted 6 days ago

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🔥 Business Intelligence Analyst - US - Remote

Posted 6 days ago

📍 United States of America

🔍 Clinical Research Organization (CRO)

5+ years of experience developing business analytics preferred.
Bachelor’s degree, preferably in Information Technology, Mathematics, or Statistics.
Understanding of Business Intelligence patterns and data modeling approaches.
Expert-level proficiency with BI tools such as Power BI, SSRS, Tableau, QlikView, and Excel/PowerPivot.
Strong communication skills and ability to work independently or in a team.
Excellent written and verbal communication skills.
Knowledge of clinical research processes and GxP regulations.

Collaborate with internal teams and stakeholders to identify and define analytics for Global Clinical Development.
Gather and prepare data from various sources including internal systems, databases, and external sources.
Consult with stakeholders to develop analyses that lead to actionable insights.
Integrate data from multiple sources to create views, track metrics, and build KPI dashboards.
Participate in the evaluation and selection of business analysis tools and software.
Produce documentation to aid in the use of published analytics.

SQLBusiness IntelligenceData AnalysisETLMicrosoft Power BIQlikViewTableauData visualizationData modeling

Posted 6 days ago

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🔥 Senior Clinical Research Associate - MidAtlatic/Northeast U.S. - Remote

Posted 9 days ago

📍 United States of America

🔍 Clinical Research Organization

5+ years of experience as a Clinical Research Associate.
A 4-year university degree or RN/BSN in Nursing.
Experience in CNS, preferably Major Depressive Disorder and Migraine.
Willingness to travel.

Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, predominantly registries and non-interventional studies.
Involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities, and managing site activities.
Conduct study initiation visits (SIVs) and ensure compliance with regulatory requirements.

Project ManagementNegotiationData management

Posted 9 days ago

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🔥 Senior Clinical Trial Manager - Oncology - U.S. Remote

Posted 9 days ago

📍 United States

🧭 Full-Time

🔍 Clinical Research

5+ years of experience as a Clinical Research Associate.
4-year university degree or RN/BSN in Nursing.
Experience as a CTM managing Oncology trials is required.
Willingness to travel is required.

Responsible for managing the research activities at sites participating in Worldwide's clinical research projects, predominantly registries and observational studies.
Involved in all stages of the clinical study including identifying potential sites, conducting study initiation visits, managing site activities during study maintenance, and closing down research activities.
Will ensure compliance with informed consent, reporting safety-related events, and adhering to regulatory requirements.

Microsoft Office

Posted 9 days ago

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🔥 Clinical Trial Liaison (Contract) - Psychiatry - U.S. Remote

Posted 10 days ago

📍 United States of America

🧭 Contract

🔍 Clinical Research Organization (CRO)

A doctoral degree, M.D., PharmD, or PhD is required.
Minimum of 5 years’ experience in clinical research in Pharma, Biotech, or CRO, including operational aspects of clinical research.
CRO experience is strongly preferred.
Minimum of 3 years’ experience in Psychiatry.
Excellent networking, written and verbal communication, negotiation, influencing, and problem-solving skills.

Establish and maintain relationships with key opinion leaders and site staff.
Conduct conversations regarding operational challenges related to patient recruitment and retention.
Hold clinical discussions with investigators to ensure study endpoint quality.
Convey feedback from KOL and site staff to internal and external teams.
Support project teams with site identification and selection.
Manage site performance issues and maintain study timelines and quality.

Problem SolvingNegotiationCritical thinking

Posted 10 days ago

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🔥 Vendor Contracts Administrator (3-month Contract) - U.S. Remote

Posted 10 days ago

📍 United States of America

🧭 Contract

🔍 Clinical Research Organization (CRO)

Excellent written and verbal communication and interpersonal skills.
Strong attention to detail.
Ability to work independently under supervision.
Ability to prioritize and handle multiple projects.
Diplomatic and professional interaction skills.
Proven resourcefulness.
Willingness to learn new systems and processes.
Strong organizational and technical skills, including proficiency in MS Word, Excel, Outlook, and Internet research.
Capability to assist in negotiation of legal and financial terms.
Data analysis/presentation experience is an advantage.
Experience in process improvement and facilitation is also advantageous.

Responsible for preparing vendor contracts by incorporating budget and scope into templates.
Review contract documents for accuracy and completeness.
Manage the contract approval/execution process and document approvals.
Track vendor contracts and supporting documentation.
Document deviations from policies and procedures.
Assist in secondary negotiations with the Director of Contracts.
Establish and maintain relationships with internal and external customers.
Handle confidential matters with discretion.
Ensure SharePoint content is monitored and updated.
Collaborate with U.S. and international offices.

Data AnalysisSharePointMicrosoft ExcelNegotiationAttention to detailOrganizational skills

Posted 10 days ago

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🔥 Senior Statistical Programmer 1 - UK/EU - Remote

Posted 25 days ago

📍 United Kingdom, Romania, Croatia

🔍 Clinical Research Organization (CRO)

Educated to degree level or equivalent.
Advanced SAS programming skills with expert knowledge in SAS/Macro, Proc Report and ODS.
Good working knowledge in SAS/Graph, Proc SQL, SAS/STAT.
Strong analytical skills and attentiveness to detail.

Develop, test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures and listings (TFL).
Serve as a programming project lead on complex studies, distribute and oversee tasks for the programming team, communicate with clients, and manage project priorities.
Perform reviews and provide guidance on clinical database specifications and data transfer agreements.
Develop and review specifications for SDTM and ADaM datasets and electronic data submission packages.

Posted 25 days ago

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🔥 Senior Clinical Research Associate - Respiratory - Midwest/Central U.S. - Remote

Posted 25 days ago

📍 United States of America

🔍 Clinical Research

5+ years of experience as a Clinical Research Associate.
4-year university degree or RN/BSN in Nursing.
Experience in Respiratory is required.
Proficiency in Microsoft Office, CTMS, and EDC Systems.
Excellent communication and organizational skills.

Responsible for managing research activities at sites participating in clinical research projects.
Involved in all stages of the clinical study from identifying potential sites to conducting study initiation visits.
Ensure compliance with informed consent and reporting of safety-related events.
Manage site activities during study maintenance and close down once studies conclude.

Posted 25 days ago

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External

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