Empleos actuales relacionados con Sr Clinical Trial Manager. Barcelona. Sponsor D161 - Madrid, Madrid - Syneos Health Clinical
-
Sr. Clinical Trial Associate
hace 3 días
Madrid, Madrid, España AIXIAL GROUP A tiempo completoSr. Clinical Trial Associate (Sr. CTA) - UK / EUJoin to apply for the Sr. Clinical Trial Associate (Sr. CTA) - UK / EU role at AIXIAL GROUPSr. Clinical Trial Associate (Sr. CTA) - UK / EUJoin to apply for the Sr. Clinical Trial Associate (Sr. CTA) - UK / EU role at AIXIAL GROUPGet AI-powered advice on this job and more exclusive features.The Aixial Group is...
-
Sr. Clinical Trial Associate
hace 7 días
Madrid, Madrid, España AIXIAL GROUP A tiempo completoSr. Clinical Trial Associate (Sr. CTA) - UK/EUJoin to apply for the Sr. Clinical Trial Associate (Sr. CTA) - UK/EU role at AIXIAL GROUPSr. Clinical Trial Associate (Sr. CTA) - UK/EUJoin to apply for the Sr. Clinical Trial Associate (Sr. CTA) - UK/EU role at AIXIAL GROUPGet AI-powered advice on this job and more exclusive features.The Aixial Group is an...
-
Clinical Trial Manager Position
hace 1 semana
Madrid, Madrid, España beBee Careers A tiempo completoJob Description:We are seeking an experienced Clinical Trial Manager to manage day-to-day operations of clinical projects, ensuring compliance with ICH/GCP and applicable laws, rules, and regulations.As a Clinical Trial Manager, you will serve as the primary sponsor contact for operational project-specific issues and study deliverables, maintaining in-depth...
-
Clinical Trial Manager
hace 1 semana
Madrid, Madrid, España beBee Careers A tiempo completoJob Description:Sponsor Dedicated Local Clinical Trial Manager IIResponsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.The ideal candidate will oversee site interactions post-activation through site closeout, including patient...
-
Sponsor Dedicated Local Clinical Trial Manager Ii
hace 4 semanas
Madrid, Madrid, España Syneos Health, Inc. A tiempo completoSponsor Dedicated Local Clinical Trial Manager II - Home Based in Madrid or Barcelona areaUpdated: December 23, 2024Location: Spain-Europe - ESP-Home-Based (Madrid)Job ID: 24006920Sponsor Dedicated Local Clinical Trial Manager II - Home Based Madrid or Barcelona area Previous CTM experience is required.Experience in Neurology, Rare disease, or Dermato/immuno...
-
Clinical Trial Assistant- Sponsor Dedicated
hace 23 horas
Madrid, Madrid, España Tn Spain A tiempo completoSocial network you want to login/join with:Clinical Trial Assistant- Sponsor Dedicated, MadridClient: IQVIALocation: Madrid, SpainJob Category: OtherEU work permit required: YesJob Views: 3Posted: 25.04.2025Expiry Date: 09.06.2025Job Description:Clinical Trial Administrator, Single Sponsor dedicated Job Overview:CTA performs daily administrative activities,...
-
Clinical Trial Associate
hace 6 días
Madrid, Madrid, España TFS HealthScience A tiempo completoJoin to apply for the Clinical Trial Associate role at TFS HealthScienceJoin to apply for the Clinical Trial Associate role at TFS HealthScienceGet AI-powered advice on this job and more exclusive features.TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies...
-
Clinical Trial Assistant- Sponsor Dedicated
hace 1 semana
Madrid, Madrid, España TN Spain A tiempo completoSocial network you want to login/join with:Clinical Trial Assistant- Sponsor Dedicated, MadridClient: IQVIALocation: Madrid, SpainJob Category: OtherEU work permit required: YesJob Views: 3Posted: 25.04.2025Expiry Date: 09.06.2025Job Description:Clinical Trial Administrator, Single Sponsor dedicatedJob Overview:CTA performs daily administrative activities,...
-
Sponsor Dedicated Local Clinical Trial Manager II
hace 20 horas
Madrid, Madrid, España Syneos Health, Inc. A tiempo completoSponsor Dedicated Local Clinical Trial Manager II - Home Based in Madrid or Barcelona area Updated: December 23, 2024 Location: Spain-Europe - ESP-Home-Based (Madrid) Job ID: 24006920 Sponsor Dedicated Local Clinical Trial Manager II - Home Based Madrid or Barcelona area Previous CTM experience is required. Experience in Neurology, Rare disease, or...
-
Madrid, Madrid, España Syneos Health, Inc. A tiempo completoSponsor Dedicated Local Clinical Trial Manager II - Home Based in Madrid or Barcelona areaUpdated: December 23, 2024Location: Spain-Europe - ESP-Home-Based (Madrid)Job ID: 24006920Sponsor Dedicated Local Clinical Trial Manager II - Home Based Madrid or Barcelona areaPrevious CTM experience is required. Experience in Neurology, Rare disease, or Dermato/immuno...
Sr Clinical Trial Manager. Barcelona. Sponsor D161
hace 3 semanas
Senior Clinical Trial Manager
Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success.
We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.
Our Clinical Development model brings the customer and the patient to the center of everything that we do.
We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.
We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture - where you can authentically be yourself.
Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with.
Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.
Job responsibilities
- Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity.
- Oversees site interactions post activation through site closeout, including patient recruitment, investigator payments or other related activities.
- Identifies critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT).
- Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/CeMs) is aware of the contractual obligations and parameters.
- Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables.
- Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope.
- Employs strategic thinking and problem-solving skills to propose and implement risk mitigations.
- Participates and presents in key meetings such as Kick Off Meeting.
- Serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members.
- Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines.
- Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities.
- Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan.
- Ensures CTMS, dashboards and other systems are set up and available for use by the clinical team, including overseeing user acceptance testing (UAT) as needed.
- Ensures access and audit trail reviews are conducted as required.
- Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans and timelines for the study.
- Oversees resourcing allocations for CRAs and Central Monitors, site assignments and study team members' conduct, and identifies risks to delivery or quality.
- Ensures quality of the clinical monitoring, central monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and / or tracking tools.
- Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboard).#J-18808-Ljbffr
