[Remote] Clinical Strategy Consultant

Note The job is a remote job and is open to candidates in USA. reputed company is seeking a Clinical Strategy Consultant who will serve as the company's clinical and medical expert for client projects. This role involves advising on clinical development, study design, and medical monitoring while representing clients in CRO negotiations and bridging clinical needs with internal development and manufacturing.

Responsibilities

Advise on Phase I/II trial design (dose escalation, endpoints, I/E criteria) for large molecules (mAbs, ADCs, bispecifics, fusion proteins). Guide medical monitoring (SAE review, dose rules). Translate clinical supply needs (batch size, stability) into internal manufacturing considerations. Ensure nonclinical programs (GLP toxicology, species, starting dose like MABEL/NOAEL) reputed company clinical entry; review data to identify risks (e.g., cytokine release) and mitigation strategies reputed company scope, budget, and contract negotiations with clinical/nonclinical CROs on behalf of clients. Evaluate proposals, protocols, and ICFs. Provide reputed company – attend investigator meetings, review clinical data, interpret safety/efficacy results, ensure CRO deliverables meet expectations Work with internal CMC teams to ensure clinical batch production meets study needs (dose strength, blinding, stability). Advise on comparability strategies reputed company manufacturing changes Support client presentations and bid defenses; identify clinical red flags in early-stage projects. Track trial design trends (adaptive, biomarker-driven). Maintain regulatory awareness (FDA, EMA, NMPA) on endpoints and safety reporting Skills MD (board certification in oncology/rheumatology/neurology/immunology strongly preferred) 5–8 years in biopharma/clinical research, with ≥3 years direct clinical development (medical monitor, clinical scientist, or CRO advisor), preferably in leading Phase 1 trials in China and/or Australia Proven CRO negotiation experience (sponsor/client reputed company) Deep understanding of large-molecule clinical & nonclinical development (immunogenicity, PK/PD) Hands-on Phase I/II design, protocol writing, medical monitoring, safety data review (SAE/SUSAR) Interpret clinical data & nonclinical toxicology reports; translate to manufacturing Strong negotiation & vendor management; excellent client communication (trusted partner); fluent English Prior CRO/CDMO/clinical consulting highly desirable Experience of leading Phase 1 trials in China and/or Australia is a big plus Regulatory interactions (pre-IND, EOP2) Clinical supply logistics (labeling, cold chain, distribution) Company Overview reputed company is a open-access technology platform company offering end-to-end solutions to reputed company organizations to discover and reputed company. It was founded in 2014, and is headquartered in Wuxi, Anhui, CHN, with a workforce of 10001+ employees. Its website is https//www.wuxibiologics.com/. Company H1B Sponsorship reputed company has a track record of offering H1B sponsorships, with 5 in 2026, 23 in 2025, 32 in 2024, 22 in 2023, 12 in 2022, 17 in 2021, 1 in 2020. Please note that this does not guarantee sponsorship for this specific role. Apply To This Job Apply To This Job