New York, USA
Email du contact:
Référence du poste:
You will be tasked with providing medical management and support as a Medical Monitor to phase 2/3 trials within the CNS / Psychiatric field. Other key duties will include;
Supporting feasibility assessments
Providing medical/clinical input to the design of study protocols and clinical development programs
Act as the global lead Medical Monitor for regional and global trials
Partner with the team members of the project team to process Serious Adverse Events (SAEs)
Provide therapeutic area and protocol-specific training to the project teams
Contribute medical expertise to the design of clinical development programs, study protocols, research papers, etc.
Support Business Development activities through participation in proposal generation, feasibility assessments, review proposals for medical services, and attendance at meetings with sponsors
Review and support the preparation of final study reports (CSRs) and other study documentation (Protocols, ISS/ISEs etc,)
Maintain a working knowledge of GCPs and regulatory requirements relating to clinical development and regulatory standards
If you are a Physician with an in depth knowledge of CNS / Psychiatric indications with previous industry experience as a Medical Monitor or Study Physician please do not hesitate to contact me.