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.

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 design of clinical studies and development of study protocols, IBs, clinical study report and other study documents to ensure compliance with regulatory requirements and GCP/ICH guidelines;

2、Be a medical monitor, manage medical and safety issues and queries derived from clinical studies;

3、Review safety data, evaluate, analyze, monitor the trend and report as appropriately;

4、Liaison with study investigators, especially investigators in China, discuss and resolve any issues which may occur during the clinical studies;

5、Provide training on study protocols, relevant diseases and medical guidelines;

6、Keep updated knowledge on the diseases related to company products and guidelines on the management of the diseases of WHO, international, and China.

1、Bachelor of Medical degree is required. Higher degree would be an advantage；

2、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、Good communication skills. Able to communicate in English fluently both in writing and orally；

5、Proven track record in clinical study design and writing study protocols and study documents；

6、Updated knowledge on oncology/immunology, and proven record as a medical monitor in clinical studies of biological product. Preferred working experience in biosimilar clinical studies；

7、Good inter-personal skills. Demonstrated ability in people management and negotiation skills；

8、Demonstrated ability in managing multiple competing priorities and problem solving. 

1、確保藥品不良反應檢測和報告的合規性，監督開展藥品安全風險識別、評估與控制，確保風險控制措施的有效執行；

2、遵照法規和公司SOP要求對不良反應/事件進行上報；

3、負責藥品安全性信息溝通的管理，確保溝通及時有效，負責藥物警戒體系的建立、運行和維護；

4、負責藥物警戒日常工作的監督和決策，完成藥品安全委員會交辦的其它藥物警戒相關工作。

1、從事上市前藥物警戒工作8年及以上，碩士及以上學歷，醫學、藥學相關專業背景；

2、熟悉國內外藥物警戒相關法律和技術指導原則，PVP優先；

3、具備藥物警戒管理工作的知識與技能；

4、有較強的溝通能力和執行能力；

5、英文讀寫熟練；熟練使用辦公軟件。

1. 協助首席注冊官共同制定注冊策略，確定注冊關鍵點，把控審批風險；

2. 負責審核及撰寫藥品注冊申報資料，確保申報品種的審評及審批進程, 及時解決或反饋該過程中出現的問題及提案；

3. 掌握項目整體進度，定期組織對項目進行階段性審核；負責對臨床全過程提供注冊法規指導及支持，指導公司項目合規開展；

4. 及時捕捉、解讀并反饋FDA注冊相關政策及產品申報信息的更新，為公司決策提供建議并在公司內部做好培訓；

5. 與相關政府機構建立良好關系，與監管機構積極溝通，促進注冊項目順利進行；

6. 建立和優化注冊法規事務相關規章制度和工作流程。

1. 醫學、藥學、生物化學、藥事管理等相關專業碩士及以上學歷；

2. 10年以上藥品注冊工作經驗，其中有3年及以上生物新藥申報經歷，有成功的IND& NDA項目申報經驗優先；

3. 熟悉藥品注冊的相關法律法規及有關藥物研究指導原則，熟悉藥品注冊申報流程和各個環節、申報資料的撰寫審核及與CFDA專家深度溝通的能力；

4. 較強的藥品注冊信息檢索和分析調研能力，能準確理解FDA、EMA等國外相關網站和文獻，英文較強讀寫能力，基本聽說能力；

5. 優秀的溝通交流與書面表達能力，具有良好的項目運作能力、分析判斷能力及解決問題的經驗，思路清晰；

6. 具有高度的責任心、原則性強，為人正直、自律，工作嚴謹。