Job Responsibilities

1. Integration & Schedule Management

-Initiate GPL preparation projects and build project teams.

-Draft project management plans, define deliverables and deadlines for each functional team.

-Track project progress, drive functional teams to deliver as scheduled, flag schedule risks, allocate resources holistically, and support teams to achieve milestone targets.

-Coordinate knowledge and document handover between R&D and commercial readiness teams after NDA submission.

-Close contracts of each phase, complete payment settlement, compile and archive project documents upon project completion or termination.

-Support project audits as required by the company.

-Prepare project presentation materials for monthly R&D management meetings, project reviews and budget hearings, and deliver presentations when needed.

2. Stakeholder Management

-Identify internal and external stakeholders and develop stakeholder management plans.

-Mobilize cross-functional resources to resolve issues.

-Hand over MAH contacts with BD/AM for in-licensing projects, and establish communication channels with MAH holders.

3. Communication Management

-Organize GPT meetings: consolidate pre-meeting materials, coordinate functional reporting during meetings, facilitate problem resolution, produce meeting minutes and follow up on action items post-meeting.

-Support GPL to escalate GPT meetings and GT decision meetings as needed, and coordinate team members to prepare meeting materials.

-Act as the primary contact for in-licensing or out-licensing projects, and coordinate meetings between project teams and external partners.

4. Budget & Procurement Management

-Develop and manage R&D budgets across phases, initiate budget approval and change processes, and present for approval at GT decision meetings and budget hearings.

-Review and support procurement workflows within projects, and monitor vendors’ performance against procurement agreements.

-Conduct regular budget actual vs. forecast analysis and cash flow forecasting.

5. Other duties assigned by department leadership, including organizing technology & innovation activities and participating in cross-functional initiatives. 

Job Requirements 

1. Education: Master’s degree or above in Clinical Medicine, Pharmacy, Pharmaceutical Affairs Management, Biological Sciences or related disciplines.

2. Professional Experience:

- Minimum 5 years of innovative drug project management experience.

-Solid understanding of drug development pathways, relevant regulations and pharmaceutical GXP systems.

- Experience managing innovative radiotheranostic drug projects.

- Track record of project management for clinical-stage assets.

3. Skills & Competencies:

- Prior experience with innovative radiotheranostic drug projects is preferred.

- Excellent writing, PPT creation, presentation and public speaking skills.

- Portfolio management experience and strong budget development & administration capabilities are preferred.

- Outstanding organizational skills, external communication, logical thinking and problem-solving abilities.

- Strong teamwork mindset, accountability and resilience under pressure.

- Proficient English in listening, speaking, reading and writing for oral and written communication with overseas partners.

- PMP certification is a plus.

Job Responsibilities:

1. Clinical Operations Oversight: End-to-end management of Phase I‑III registered clinical trials (including IITs) for radiopharmaceuticals. Develop and maintain clinical project plans, timelines, budgets and resource plans; lead milestone delivery, risk control for trial initiation, execution and close-out.

2. Radiopharmaceutical Coordination: Oversee radiopharmaceutical manufacturing, QC, transportation within decay windows and on-site storage at study sites to ensure radiation safety and timeline compliance.

3. Study Site Management: Manage SSU and multi-site operations (site feasibility, ethics submission, site initiation, enrolment, monitoring and close-out). Supervise daily site performance including enrolment rates, protocol adherence and quality assurance in compliance with GCP and study protocols. Organize investigator meetings, site training and prepare for audits / regulatory inspections.

4. Vendor & Cross-functional Collaboration: Manage CRO/SMO, central laboratory and logistics vendors; collaborate with internal medical, CMC and regulatory teams. Maintain eTMF/TMF systems.

5. Safety & Risk Management: Monitor SAEs and radiation safety; report project progress and risks to management on a regular basis.

Job Requirements:

1. Education: Bachelor’s degree or above in Pharmacy, Nuclear Medicine, Life Sciences or related fields.

2. Professional Experience:

- Minimum 5 years of clinical trial operations experience, with at least 2 years independently leading clinical projects.

- Full lifecycle ownership of ≥1 radiopharmaceutical clinical project; candidates with experience on nuclides such as ¹⁷⁷Lu / ²²⁵Ac are highly preferred.

- Familiarity with radiopharmaceutical CMC and supply chain (GMP manufacturing, cold chain, delivery decay windows).

- Knowledge of GCP, NMPA regulations and radiopharmaceutical / radiation safety requirements.

- Hands-on experience with EDC / CTMS / eTMF systems.

Job Responsibilities：

1. Independently lead early‑stage medicinal chemistry R&D for innovative drugs, conduct end‑to‑end R&D experiments including molecular design, synthesis, structural modification, purification and characterization, optimize experimental processes, resolve technical challenges during R&D, and ensure smooth project execution.

2. Apply Computer‑Aided Drug Design (CADD) technologies for molecular screening, structure‑activity relationship (SAR) analysis and structural optimization to improve compound druggability and safety, and effectively support new‑drug discovery.

3. Formulate experimental protocols and schedules in accordance with corporate R&D strategies, independently drive R&D projects, strictly control experimental quality and project milestones, review experimental data, identify and address R&D bottlenecks, and guarantee delivery of phase‑specific project goals on schedule.

4. Standardize R&D data archiving, organize research outputs, compile lab notebooks, project summaries, technical reports and other R&D documents, and support patent filing and achievement‑application activities.

5. Collaborate cross‑functionally with pharmacology, analytical chemistry, CMC and other departments for project delivery; keep abreast of cutting‑edge R&D technologies in the industry, optimize R&D workflows, and assist in mentoring junior R&D staff.

Job Requirements： 

1. Education & Professional Experience

Majors in Medicinal Chemistry, Organic Chemistry, Pharmaceutical Engineering or other chemistry‑ / pharmacy‑related disciplines. Master’s degree or above, with no less than 5‑year new‑drug R&D experience for master holders, or no less than 2‑year new‑drug R&D experience for PhD holders. Prior working experience in innovative‑drug biotech companies is preferred.

2. Core Competencies

Proficient in standard R&D workflows including drug synthesis, purification and structural characterization; skilled in operation and data analysis of instruments such as HPLC and LC‑MS. Capable of operating CADD software for molecular screening and structural optimization. Prior hands‑on experience in peptide‑based drug or radiopharmaceutical projects is a plus.

3. Professional Capability

Solid expertise in medicinal chemistry, familiar with early‑phase new‑drug discovery workflows. Capable of independently solving technical hurdles and taking full ownership of R&D projects.

4. Comprehensive Qualities

Strong capabilities in literature research, data analysis and report summarization. Meticulous and responsible work attitude, good communication, collaboration and project‑delivery skills. Able to adapt to R&D work rhythms and withstand work pressure.

5. Preferred Qualifications

Proven track record of end‑to‑end pre‑clinical new‑drug projects and IND‑enabling experience; candidates with relevant patents or high‑quality publications are preferred.