1. According to Doma’s corporate and portfolio strategy, explore collaboration opportunities with the partners.

2. Support Due Diligence，coordinate with PM and R&D head to ensure project quality and timeline, negotiate contract;

3. Brand Doma via various channels and seek potential partnership;

4. Keep up with the latest market and industry development landscape, Work closely with leaders and cross-functional management team members to design and execute the Doma’s business development strategy. 

1. Master degree or above in biology, other relevant fields, at least 3+ years’ Business Development industrial working experience in biotech and/or pharmaceutical companies;

2. Strong communication skills in English and ppt drafting，able to work independently and a strong team player;

3. Prefer consulting background, good at communication & impact on internal and external stakeholders;

4. Excellent presentation skill both written and oral;

5. Familiar with BD process and good at negotiation;

6. Self study and curious in new science;

7. Familiar with financial analysis.

1. Responsible for the conduct of assigned clinical studies, including clinical study plan, CRO activities, project timelines and budget, management of Consultants/Advisors and any other related activities.

2. Ensure the clinical studies are carried out in accordance with regulatory requirements, ICH and GCP principals.

3. Participate in selection of study vendors and keep good working relationship with the selected vendors to ensure the status of clinical studies is up-to-date, issues are attended and resolved timely, and the clinical studies are progressing according to plan.

4. Identify and provide solutions to clinical issues and risks. Any unresolved issues are escalated appropriately.

5. Coordinate internal and external clinical development activities of team members involved in the design and conducted of clinical trials.

6. Ensure any safety issues AEs/SAEs are properly managed and reported according to regulatory requirements.

7. Ensure all clinical study related SOPs are in place and updated according to GCP requirements.

8. Contributes to relevant study documentation including protocols, data review, statistical analysis plan, clinical study reports and operational plans.

9. Oversees submission of trial-related and essential documents to Trial Master File.

10. Provide training to junior staff as required.

1. BS or Master’s degree in nursing, life science, or medical/pharmacy related fields.

2. 5~8 years of relevant clinical research experience in a pharmaceutical company or CRO.

3. Thorough knowledge of ICH, and GCP guidelines, clinical study process and procedures, and reporting of AEs/SAEs.

4. Proven track record showing clear proficiency in clinical project management skills and broad understanding of clinical operations, and CRO/vendors management skills.

5. Good communication skills, both oral and writing. Fluent in English.

6. Good inter-personal skills. Demonstrated ability to successfully participate as a member of a project team.

7. Demonstrated ability in managing multiple competing priorities and problem solving.