Company

Biotech

Principal,GlobalFeasibility(pre-awardstrategy)

$175–250k ~AI est. Switzerland FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Principal, Global Feasibility (pre-award strategy). Skills: Global feasibility, Pre-award strategy, Clinical trial execution. Lead feasibility assessments. Deliver feasibility assessments”

Industry & Context.

Biotech
Problems you'll solve

Analytical thinking; Strategic thinking; Problem-solving skills

What They're Looking For.

Must Have

7+ years experience (BS/RN/MS), 3+ years experience (PhD/MD), Clinical research background, GCP understanding, Study start-up processes, Global clinical feasibility knowledge, Country and site selection knowledge, Drug development lifecycle knowledge, Manage complex workloads, Manage multi-study workloads, Work under tight deadlines, High attention to detail, Synthesize complex data sets, Influence effectively, Negotiate effectively, Work effectively in global teams, Customer-facing roles experience, Consultancy-style roles experience, Manage competing priorities, Fast-paced environment experience

Nice to Have

Advanced degree in Life Sciences

What You'll Do.

Lead feasibility assessments

Deliver feasibility assessments

Lead pre-award strategy assessments

Deliver pre-award strategy assessments

Develop site-level feasibility outputs

Analyze site-level feasibility outputs

Present site-level feasibility outputs

Design feasibility strategies

Identify innovative solutions

Propose innovative solutions

Conduct advanced research

Support bid defense preparation

Participate in client-facing meetings

Maintain accurate documentation

Ensure high-quality data management

Contribute to departmental metrics development

Contribute to feasibility frameworks development

Contribute to process improvements

Mentor junior team members

Support junior team members

Mentor mid-level team members

Support mid-level team members

Provide guidance on analysis

Provide guidance on reporting

Provide guidance on best practices

Participate in strategic initiatives

Participate in system development

Participate in data asset evaluation

Participate in methodology improvement

How You'll Work.

Team & Collaboration

Cross-functional teams; Global teams

Communication Scope

Written communication; Verbal communication; Presentation abilities; Senior stakeholder engagement

Process & Methodology

Workload management

Full Job Description

## Accountabilities Lead and independently deliver highly complex global feasibility and pre-award strategy assessments across all therapeutic areas, including RFP and partnership feasibility work. Develop, analyze, and present site-level feasibility outputs in both written and presentation formats for internal and external stakeholders. Collaborate cross-functionally with business development, medical directors, business analysts, and operational teams to design optimal feasibility strategies. Identify and propose innovative solutions for non-standard or complex feasibility requests with minimal supervision. Conduct advanced research using scientific literature, internal data systems, and external sources to support evidence-based feasibility decisions. Support bid defense preparation and participate in client-facing meetings with a high level of professionalism and autonomy. Maintain accurate documentation and ensure high-quality data management within internal systems and knowledge repositories. Contribute to the development of departmental metrics, feasibility frameworks, and process improvements to enhance operational efficiency. Mentor and support junior and mid-level team members, providing guidance on analysis, reporting, and best practices. Participate in strategic initiatives, including system development, data asset evaluation, and continuous improvement of feasibility methodologies. Requirements Advanced degree in Life Sciences or related field (BS/RN/MS with 7+ years of experience, or PhD/MD with 3+ years of relevant experience). Strong background in clinical research, including clinical trial execution, GCP understanding, and study start-up processes. Deep knowledge of global clinical feasibility, country and site selection, and drug development lifecycle. Proven ability to independently manage complex, multi-study workloads under tight deadlines while maintaining high attention to detail. Strong analytical, strategic thinking, and problem-solving skil

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