Senior Manager/Associate Director/Director/Senior Director
Job Responsibilities
1.Take lead or contribute to developing clinical development plan for the assigned project;
2.Accountable for clinical study protocol development and medical monitoring related activities;
3.Support preparation of study related documents (e.g. IB, study protocol, ICF, CRF, SMC charter, medical monitoring plan, SAP, CSR);
4.Support clinical safety reviews and data analyses;
5. Interact and collaborate with external service providers and expert consultants.
Qualifications:
1.Medical degree (M.D.) with good medical knowledge and clinical experience in neurology or chronic pain, Master or Ph.D would be a plus;
2. At least 3 years of industry experience in clinical research;
3.Good command of English, both in written and spoken.
E-mail:hr@simrbio.com