7 Jobs für Travel Manager CTM
Stellenangebote Travel Manager CTM Jobs
Job vor 9 Tagen bei Jooble gefunden
Linical
• Deutschland Deutschland, DE
[. .. ] dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while [...]
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[...] the Clinical Operations Manager (COM) will oversee the CRA role. Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and associated documentation; participates in the final selection of investigative sites Conducts site initiation visits; trains site [. .. ] and tools; participates in development of participant tracking systems; conducts monitoring assessment visits for the purpose of rescuing a troubled site or performing audit preparation at the direction of the CTM Senior CRA oversees work for assigned CRAs on a designated project; reviews and approves monitoring visit reports; manages the visit schedule; provides feedback during the annual review process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience [. .. ] and ability to work successfully in a matrixed team environment Dedication to quality in all work tasks and deliverables Ability to prioritize and manage multiple tasks as necessary, including during travel and monitoring visits Working knowledge of computer systems, applications, and operating systems Ability to travel up to 75 Possess a valid drivers license, as required 90137939 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
[. .. ] part of a stable, well-established organization with long-term career opportunities Strong collaboration with experienced CTMs and project teams Clear development pathways (e. g. , Senior CRA, Lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRA, CTM) Flexible working models that support work-life balance Permanent employment Full-time (40 hours/ week) About the Role This position is for experienced Clinical Research Associates with 2+ years of independent monitoring experience. You will manage clinical trial sites across Germany, ensuring studies are conducted in compliance with the protocol, [. .. ] to support issue resolution and data quality Ensure study systems (e. g. , CTMS) are updated according to study conventions Provide trial status updates and metrics to the Clinical Team Manager (CTM) Support study start-up, investigator identification, site initiation, and study close-out activities as assigned Participate in investigator meetings, audits, inspections, and project team meetings as required Additional responsibilities may include supporting process improvement initiatives, mentoring activities, or project-specific tasks aligned with experience. A Day in the Life [. .. ] Proficiency in Microsoft Office and ability to learn clinical systems (e. g. , CTMS) Locations: Home-based or hybrid anywhere in Germany FTE: Full-time (40 hrs/ week) Contract: Permanent Travel: Approximately 5075 (study-dependent) At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will [. .. ]
Job am 08.04.2026 bei Jooble gefunden
ICON
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
As a
Manager, Site Engagement Liaison, you will be joining the worlds largest most comprehensive clinical research organisation, powered by healthcare intelligence. The Site Engagement Liaison Manager is a field [...]
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[...] based expert who supports the conduct and the patient recruitment of the client global clinical trials at investigative sites, through local and relational [. .. ] and pro-actively identify ways to prevent recruitment delays Pro-actively identify issues and look for solutions in the assigned clinical trial and timely escalate them to the respective study CTM, CODL, Global Head of Clinical Site Communication, Recruitment and Liaisons, Head of Trial Operations and/or Senior Management, as needed Identify efficiencies, best practices and lessons learnt and ensure they are shared across trials/ indications/ compounds Search for and embrace innovation May be asked to provide input to the clinical [. .. ] of 6 years of experience in Biotech/ pharma preferably in roles including site engagement and/or clinical trial monitoring experience Experience as Lead CRA, Manager is an asset. Ability for travel nationally and occasional international travel. Experience in global clinical trials is a plus Prior experience in Neurology, Auto-immune and rare disease background Knowledge of ICH-GCP and other applicable legislation Ability to quickly understand complex neurological disease areas, treatments and clinical development plans Understand the healthcare therapeutic landscape, patient [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
[. .. ] part of a stable, well-established organization with long-term career opportunities Strong collaboration with experienced CTMs and project teams Clear development pathways (e. g. , Senior CRA, Lead [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRA, CTM) Flexible working models that support work-life balance Permanent employment Full-time (40 hours/ week) About the Role This position is for experienced Clinical Research Associates with 1+ years of independent monitoring experience. You will manage clinical trial sites across Germany, ensuring studies are conducted in compliance with the protocol, [. .. ] to support issue resolution and data quality Ensure study systems (e. g. , CTMS) are updated according to study conventions Provide trial status updates and metrics to the Clinical Team Manager (CTM) Support study start-up, investigator identification, site initiation, and study close-out activities as assigned Participate in investigator meetings, audits, inspections, and project team meetings as required Additional responsibilities may include supporting process improvement initiatives, mentoring activities, or project-specific tasks aligned with experience. A Day in the Life [. .. ] Proficiency in Microsoft Office and ability to learn clinical systems (e. g. , CTMS) Locations: Home-based or hybrid anywhere in Germany FTE: Full-time (40 hrs/ week) Contract: Permanent Travel: Approximately 5075 (study-dependent) At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will [. .. ]
Job am 08.04.2026 bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Local Clinical Trial
Manager-Single Sponsor Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug [...]
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[...] development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug [. .. ] can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities For one of our single sponsor clients we are looking for CTM to cover phase II/ III trials. 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. This may include patient recruitment, investigator payments or other related activities. May [. .. ] identifying and mitigating potential threats to the successful conduct of a clinical research project. Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues Moderate travel may be required, approximately 25 Get to know Syneos Health Over the past 5 years, we have worked with 94 of all Novel FDA Approved Drugs, 95 of EMA Authorized Products and over 200 Studies across 73, 000 Sites and 675, 000+ Trial patients. No matter what your role is, [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate-Germany
• München, Bayern
[. .. ] dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Clinical Operations Manager (COM) will oversee the CRA role. Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and associated documentation; participates in the final selection of investigative sites Conducts site initiation visits; trains site [. .. ] and tools; participates in development of participant tracking systems; conducts monitoring assessment visits for the purpose of rescuing a troubled site or performing audit preparation at the direction of the CTM Senior CRA oversees work for assigned CRAs on a designated project; reviews and approves monitoring visit reports; manages the visit schedule; provides feedback during the annual review process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience [. .. ] and ability to work successfully in a matrixed team environment Dedication to quality in all work tasks and deliverables Ability to prioritize and manage multiple tasks as necessary, including during travel and monitoring visits Working knowledge of computer systems, applications, and operating systems Ability to travel up to 75 Possess a valid drivers license, as required #J-18808-Ljbffr 90460783 [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
This role reports to the Operations Team
Manager. This role is full time, fully remote or hybrid from our Berlin office. Working hours for this role are Monday to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Friday, 40 hours per week. CTM is an award-winning provider of travel service solutions for the corporate, events and sports markets. Headquartered and founded in Australia, we have a global presence, with offices in Europe, Asia, North America, Australia New Zealand. We have an exciting opportunity for you to join our crew and take your career to new altitudes. The role Working [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Travel Manager CTM pro Jahr?
Als Travel Manager CTM verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Travel Manager CTM Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 7 offene Stellenanzeigen für Travel Manager CTM Jobs.
In welchen Bundesländern werden die meisten Travel Manager CTM Jobs angeboten?
Die meisten Stellenanzeigen für Travel Manager CTM Jobs werden derzeit in Bayern (2 Jobs), Berlin (1 Jobs) und Nordrhein-Westfalen (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Travel Manager CTM Jobs?
Travel Manager CTM Jobs gehören zum Berufsfeld Reisen, Tourismus, Hotellerie, Gastronomie.
