Clinical Trial Manager

Lawrence Harvey

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Job ID :


Company Type :

Staffing Firms

Industry :


Education Level :


Address 1 :

North America,--California,South San Francisco,

Key Skills :

Clinical Trial Manager

Salary :


Date Posted :

31 Jul, 2017

Company Name :

Lawrence Harvey

Location1 :

South San Francisco

Job Category :

Clinical Research Jobs

Experience :


Job Type:


Travel Amount:

upto 15%


Clinical Trial Manager

Redwood City/ Palo Alto/ San Jose/ LA

SciPro Global are currently looking for a Clinical Trial Manager based in the Greater Boston Area or willing to relocate- full relocation package available.

As the Clinical Trial Manager you will be responsible for executing clinical strategies to deliver successful operational outcomes across multiple clinical trials. In addition to exceptional project delivery, we seek strong analytical skills and leadership qualities that will influence our internal team and motivate our CRO partners.

The ideal candidate values bringing important medicines to patients in need, and shares our team's determined, positive attitude.


* Regularly interacts with Clinical Affairs and company leadership on matters concerning clinical development status.
* Devises efficient, effective clinical trial execution strategies; guides planning and execution of clinical studies, including management of study budgets, timelines, and external vendor(s) management.
* Proficient in clinical trial timeline and budget forecasting, using objective measures and tools to plan and communicate key clinical trial metrics.
* Exceptional planning, communication, and creative problem solving skills, ensuring trial delivery for one or more clinical trials.
* Leads by example and mentors other Clinical Operations team members, including employee development through company goal setting, performance management processes.
* Ensures compliance of clinical trials with federal and applicable regulatory agency requirements.
* Assists in the development and implementation of policies and standard operating procedures (SOPs) to be used in Clinical Operations.
* Integrates best practices as appropriate.


* BS/MS in a science or a health-related field.
* 4 - 8 years of related work experience, with at least 4 years in a study management role.
* Biopharmaceutical (Sponsor) organization experience is a must. CRO experience is also desirable.
* Experience managing and training regional or consulting CRAs within project teams is required; direct line management is not required
* In-depth knowledge of the CRO selection and contracting processes
* Must have thorough understanding of GCP and ICH regulations, clinical trial monitoring, and regulatory compliance.

If this is something you would be interested in, please apply directly or you can send your contact details and avaiability to

Company Name:

Lawrence Harvey


150 Leadenhall Street,London


Staffing Firms


United Kingdom





100 - 499


Pharmaceutical Recruitment



Phone No. :

0203 327 3072

Lawrence Harvey Life Sciences has exceptional relationships with the top talent and leading organisations in the Pharmaceutical and Medical Devices industry across the UK, USA, DACH region and the rest of Europe. Our consultants are experts within their specific areas and have a deep understanding of the full Life Sciences developmental cycle. As a client with a challenging role or a candidate with a niche specialism, you will receive a consultative service from people who truly understand the expectations and requirements of your industry. In an ever developing industry, an in-depth technical understanding and knowledge adds significant value and is imperative to ensuring our consultants are always up to speed, positioning ourselves perfectly to offer advice, analysis and support to our clients and candidates. We partner with leading pharmaceutical, medical device, generics, biotechnology, clinical research, R&D, manufacturing, regulatory affairs, CRO’s, CMO’s and medical communications organisations and have acquired an enviable and unrivalled reputation for delivering on niche, hard to fill and challenging positions. Our Specialisms within Life Sciences: Pharmaceuticals Medical Devices Regulatory Affairs Quality Assurance Quality Control Engineering Medical Affairs / Medical Information Qualified Persons Drug safety & Pharmacovigilance Biostatistics Clinical SAS Medical Writing Account Management & Business Development

For more information,visit

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