Senior Manager, Clinical Scientist

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Position Summary-.

Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct.

May serve as Clinical Trial Lead for one or more trials.

May lead or support trial level activities for one or more trials with the necessary supervision.

May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members.

Resposibilities-QualificationMD Degree in life sciences is mandatory.

Collaborate and liaise with external partners (eg, KOLs).

Seek out and enact best practices with instruction.

Provide regular and timely updates to manager/management as requested.

Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required.

Conduct literature review.

Submit clinical documents to TMF.

Develop site and CRA training materials and present these at SIVs and Investigator meetings.

Review clinical narratives.

Monitor clinical data for specific trends.

Develop Data Review Plan in collaboration with Data Management.

Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming.

Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (eg, IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission. ).

Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.

Ability to understand assigned protocol(s) and their requirements.

Basic knowledge skills to support program-specific data review and trend identification.

Intermediate medical writing skills and medical terminology.

Basic planning/project management skills (develop short range plans that are realistic and effective).

Oncology and Hematology Exposure is compulsory.

Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.

Ability to understand assigned protocol(s) and their requirements.

Basic knowledge skills to support program-specific data review and trend identification.

Intermediate medical writing skills and medical terminology.

Basic planning/project management skills (develop short range plans that are realistic and effective).