8 Jobs für Interim Supervisor
Stellenangebote Interim Supervisor Jobs
Job am 08.04.2026 bei Jooble gefunden
Optimapharm d. o. o.
• Hessen Hessen, DE
[. .. ] work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Your responsibilities Perform routine site visits independently, including pre-study, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying [. .. ] each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Optimapharm d. o. o.
Clinical Research Associate II/ III-Germany
• Berlin Berlin, DE
[. .. ] work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Your responsibilities Perform routine site visits independently, including pre-study, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying [. .. ] each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Optimapharm d. o. o.
Clinical Research Associate II/ III-Germany
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
[. .. ] work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Your responsibilities Perform routine site visits independently, including pre-study, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying [. .. ] each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Optimapharm d. o. o.
Clinical Research Associate II/ III-Germany
• Westfalen Westfalen, DE
[. .. ] work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Your responsibilities Perform routine site visits independently, including pre-study, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying [. .. ] each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If [. .. ]
Job am 05.04.2026 bei Jobleads gefunden
Clinical Research Associate II/ III-Germany
• Berlin
[. .. ] skills Ability to work independently, proactive Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Responsibilities Perform routine site visits independently, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] including prestudy, initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identify and escalate potential risks and identify [. .. ] of each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of studyrelated documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fastgrowing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If you [. .. ]
Job am 14.03.2026 bei Jobleads gefunden
Clinical Research Associate II/ III-Germany
• Frankfurt, Hesse
[. .. ] work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Your responsibilities Perform routine site visits independently, including pre-study, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying [. .. ] each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Clinical Research Associate II/ III-Germany
• Berlin
[. .. ] work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Your responsibilities Perform routine site visits independently, including pre-study, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying [. .. ] each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If [. .. ]
Job am 11.03.2026 bei Jobleads gefunden
Clinical Research Associate II/ III-Germany
• Frankfurt, Hesse
[. .. ] work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid drivers license Your responsibilities Perform routine site visits independently, including pre-study, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying [. .. ] each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable) , and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/ institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Interim Supervisor pro Jahr?
Als Interim Supervisor verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Interim Supervisor Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 8 offene Stellenanzeigen für Interim Supervisor Jobs.
In welchen Bundesländern werden die meisten Interim Supervisor Jobs angeboten?
Die meisten Stellenanzeigen für Interim Supervisor Jobs werden derzeit in Berlin (3 Jobs), Hessen (2 Jobs) und Sachsen-Anhalt (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Interim Supervisor Jobs?
Interim Supervisor Jobs gehören zum Berufsfeld Unternehmensberatung.
