Remote Global Clinical PM II — Hematology

Syneos Health; Amsterdam; On-site; EUR 95,000 - 129,000; Full time

Job summary

Syneos Health is seeking a Global Clinical Project Manager II for late-phase Hematology/Immunology portfolios. This fully home-based role requires sponsor-side and global study experience, with expertise in Oncology, Hematology, or Immunology and a track record with complex or pivotal studies.

You will support the Clinical Trial Manager and operations teams, liaise with CROs and vendors, and contribute to study documents, master ICF templates, and risk amendments in a dynamic, globally

Qualifications

• Prior sponsor-side experience.
• Global study experience, rather than experience limited to a single region.
• Oncology, Hematology, or Immunology therapeutic area expertise, ideally with experience supporting complex or pivotal studies.

Responsibilities

• The PM II provides supporting services to the Clinical Trial Manager/operational team in execution of the trial(s). These services include direct liaison with CROs and other ancillary vendors, as appropriate, to manage relevant trial(s) operational tasks.
• The Lead maintains effective communication with the project team through oral and written correspondence and status reports to ensure alignment with study timelines.
• Reviewing, developing, and writing clinical trial documents and manuals, including study manuals, laboratory or biomarker plans, and other supporting documents.
• The creation of the Master ICF template and review/approve site changes (in consultation with legal, safety when warranted), plus update template for new risks and new amendments information.

Skills

Sponsor-side experience

Global study experience

Oncology/Hematology/Immunology

Pivotal studies experience

Job description

Syneos Health is seeking a Global Clinical Project Manager II for late-phase Hematology/Immunology portfolios. This fully home-based role requires sponsor-side and global study experience, with expertise in Oncology, Hematology, or Immunology and a track record with complex or pivotal studies.

You will support the Clinical Trial Manager and operations teams, liaise with CROs and vendors, and contribute to study documents, master ICF templates, and risk amendments in a dynamic, globally