Clinical Scientist – Oncology (Medical Monitoring | Phase III | Remote)
Job Title- Clinical Scientist I
Location: Basking Ridge, NJ 07920 (Remote)
Duration: Contract till Oct 2026 with possibility to extend
Checklist
Medical monitoring, medical monitoring activities of a large Ph3 study -
Oncology clinical trials -
Direct pharma experience -
Biology, pharmacy, biotechnology or equivalent. PharmD/Phd preferred -
Duties
Job Title: Clinical Scientist
Job Schedule: -Candidate is able to work 100% remote as they can work EST hours (note - there will be 7am start of meetings at times).
We are seeking an experienced Clinical Scientist to support the medical monitoring and execution of oncology clinical trials from April to October 2026. The role can be based in the US remote and requires close collaboration with cross-functional teams in a dynamic and fast-paced environment.
The successful candidate will be supporting medical monitoring activities of a large Ph3 study, focusing on the review of patient profiles, patient data, patient listings, safety data, query management and protocol compliance. The candidate will contribute to the ongoing evaluation of clinical data, support issue resolution, and ensure the scientific integrity of the trial. The role involves regular interaction with Clinical Science, Clinical Operations, Data management, Statistical team, investigators, and other stakeholders to provide medical and scientific input during study conduct.
Candidates should have a strong background in the lifescience field, with a PharmD or PhD preferred, and a minimum of a Bachelor’s degree in a relevant field. A solid experience in oncology clinical trials, particularly in medical monitoring, is required, with at least 3 years of hands-on experience. Familiarity with the environment or prior experience as a contractor within is considered an advantage.
The ideal candidate is a team player, flexible and proactive, with strong analytical and communication skills. Fluency in English is required.
Skills
• Clinical Scientist or equivalent experience
-at least 2-3 years experience in medical monitoring
-solid experience in medical monitoring of clinical studies in oncology
• advantage if the candidate is familiar with DS environment / prior contractor in DS
-from April until October 2026
-team player, flexible, proactive, fluent in English
Education
Minimum of completed B.Sc. in the lifescience field (biology, pharmacy, biotechnology or equivalent). PharmD/Phd preferred but optional.
Location: Basking Ridge, NJ 07920 (Remote)
Duration: Contract till Oct 2026 with possibility to extend
Checklist
Medical monitoring, medical monitoring activities of a large Ph3 study -
Oncology clinical trials -
Direct pharma experience -
Biology, pharmacy, biotechnology or equivalent. PharmD/Phd preferred -
Duties
Job Title: Clinical Scientist
Job Schedule: -Candidate is able to work 100% remote as they can work EST hours (note - there will be 7am start of meetings at times).
We are seeking an experienced Clinical Scientist to support the medical monitoring and execution of oncology clinical trials from April to October 2026. The role can be based in the US remote and requires close collaboration with cross-functional teams in a dynamic and fast-paced environment.
The successful candidate will be supporting medical monitoring activities of a large Ph3 study, focusing on the review of patient profiles, patient data, patient listings, safety data, query management and protocol compliance. The candidate will contribute to the ongoing evaluation of clinical data, support issue resolution, and ensure the scientific integrity of the trial. The role involves regular interaction with Clinical Science, Clinical Operations, Data management, Statistical team, investigators, and other stakeholders to provide medical and scientific input during study conduct.
Candidates should have a strong background in the lifescience field, with a PharmD or PhD preferred, and a minimum of a Bachelor’s degree in a relevant field. A solid experience in oncology clinical trials, particularly in medical monitoring, is required, with at least 3 years of hands-on experience. Familiarity with the environment or prior experience as a contractor within is considered an advantage.
The ideal candidate is a team player, flexible and proactive, with strong analytical and communication skills. Fluency in English is required.
Skills
• Clinical Scientist or equivalent experience
-at least 2-3 years experience in medical monitoring
-solid experience in medical monitoring of clinical studies in oncology
• advantage if the candidate is familiar with DS environment / prior contractor in DS
-from April until October 2026
-team player, flexible, proactive, fluent in English
Education
Minimum of completed B.Sc. in the lifescience field (biology, pharmacy, biotechnology or equivalent). PharmD/Phd preferred but optional.