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Job Details

Clinical Project Manager

Company: DOCS Global
Location: Princeton, New Jersey
Reference: US- JHPM01
Closing Date: 21 Mar 18
Type: Full Time
Salary (£): On Application
Benefits: Perm Benefits

Job Summary:

DOCS are hiring Clinical Project Manager to work in an embedded team with their FSP client. This is an exciting and unique opportunity to help mold and grow this new division from the beginning. We are looking to hire Clinical Project Managers who are hardworking, passionate and focused on delivering innovation and seeking out opportunity.

Requirements:

Main responsibilities

Assists and / or contributes to the successful and timely execution of a clinical research protocol from study start up to final clinical study report.

Executes targeted activities with direction from the Protocol Manager or other team members to contribute to the overall project.

These activities may include but are not limited to:

  • Tracking of timelines
  • Maintenance of project plan
  • Any Prior Pharma/Biotech Sponsor employment                                                
  • Negotiation skills     
  • Managing Budgets and timelines                                                                           
  • Ability to work on multiple projects simultaneously                                                                                     
  • Flexible/adaptable to changing priorities                                           
  • Strong relationship (internal and external) management                     
  • Project management experience  / Global Projects                                                               
  • Site monitoring or management experience    
  • Any prior experience in non interventional studies and investigator sponsor research is a plus
  • Maintenance of study files
  • Collection, review and filing of regulatory documents
  • Assisting with meeting planning including documentations of meeting minutes / action items
  • Preparation of data for annual reports
  • Review of narratives
  • Co-ordinating the development of protocol level documents and plans
  • Clinical supply oversight
  • Vendor oversight/ Multi-Vendor experience
  • Enrolment tracking
  • Clinical data review and cleaning
  • Contributing to audit responses
  • Updating of various trial management systems
  • Study close out

 

Experience Required

Essential

  • Minimum of BA/BS Degree, or equivalent, from accredited institution                                                                                                             
  • 2-4 years demonstrated clinical trial management experience for junior personnel
  • Thorough understanding of ICH/GCP guidelines and regulations
  • Experience in all phases of study execution/protocol management
  • Experience in developing key study documents, such as protocol, informed consent form, clinical study report
  • Knowledge of pharmaceutical industry regarding pre-clinical, clinical, regulatory and commercial components
  • Strong written and verbal communication skills
  • Strong interpersonal and organizational skills, ability to multitask
  • Ability to work on site in Lawrenceville

Desirable

  •  TA Experience in Oncology, CV, Immunology, Virology
  •  Knowledge of Clinical Trial Management Systems
  •  Knowledge of project management principles
  •  Currently employed; unemployed individuals considered if Degree/Experience and Relevant

Salary & Package

  • A world-class research environment
  • Strong culture of recognition and support
  • Great work-life balance
  • Strong ability to get involved, grow in role and gain visibility
  • Anyone in NY area that may be interested there is a train and BMS shuttle to assist with commute
  • Ability to work towards 2 days a week from home (1 day after 3-6 months up to a maximum of 2 days after 6 months)
  • A uniquely collegial working culture
  • Salary: Competitive


If you are seeking an international company who is committed to development and training and the opportunity for career progression, please get in contact.

Pharmaceutical, clinical trials, clinical research, study manager, site manager, study start up, clinical study report, protocol management, clinical components, study execution, Project Management, Global Experience, Multi-vendor experience

 

Apply for this job: Clinical Project Manager

Contact Information:

Address:  DOCS International
Pinewood
Chineham Business Park
Chineham
Hampshire,
United Kingdom
RG24 8AL
England
Reasons to work for Docs International
Tel:  +44 (0) 1256 698004
Website:  Visit Our Web Site

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