Clinical Project Manager job in New York, USA

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Last Name*

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First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

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Phone Number*

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Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: CRA Manager, Project/Study Manager (CSM/CPM), Program Manager / Director

Location: United States

This vacancy has now expired

Proclinical is currently recruiting for a Clinical Project Manager with a leading CRO located in New York, NY. As a Clinical Project Manager, you will be responsible for managing the execution of the company's growing portfolio of POC, Phase II, and real-world evidence studies.

Job Responsibilities:

Use industry knowledge, experience, and first-principles thinking to refine our strategy for delivering key study services, with a primary focus on Project Management.
Lead execution of the company's initial portfolio of POC, Phase II, and real-world evidence studies, including oversight of trial performance, management of vendors, and leadership of cross-functional study teams.
Develop clinical trial timelines and budgets, and ensure study teams deliver against time, quality, and cost targets.
Partner with cross-functional teams from Operations, Data Management, Medical, Engineering, QA, and more to develop capabilities.
Represent the company to study sponsors, including driving reporting and updates.
Partner with Sales, Marketing, and other internal teams to define how we go to market and support new business pitches.
Lend industry expertise across the company, helping us plot our route toward making clinical trials faster, more efficient, and higher quality.

Skills and Requirements:

BS required, preferably in life sciences or a related field; advanced degree preferred.
5 - 8 years' biopharma industry experience.
3+ years of clinical project management experience at a biopharma company or CRO.
Demonstrated ability to plan and lead teams in executing complex global clinical trials.
Deep experience with all aspects of study management, including feasibility, study planning and budgeting, study resourcing, vendor management, risk management, stakeholder management, and more.
Thorough knowledge and understanding of clinical research concepts, practices, and regulations.
Critical thinker with ability to step back and rethink legacy assumptions in the clinical research space; should be able to point to what's wrong, and how you would do it differently if starting from scratch.
Excellent cross-functional partnership skills; you know how to work across an organization to achieve objectives and meet timelines.
Solid written and oral communication skills; can synthesize complex concepts and deliver messages clearly.
Competency with data analysis: should have intermediate+ ability with Excel, and fluency with managing to metrics and key performance indicators.
Preferably located in the greater New York metro area or willing to relocate. If remote, must be willing to travel to the NYC office on a regular basis.

If you are having difficulty in applying or if you have any questions, please contact Paige Sanderson at (+1) 646-367-2618 or p.sanderson@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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