Project Director - Home Based vacancy at Ockham Development Group Inc in Tampa

Ockham Development Group Inc is currently interviewing Project Director - Home Based on Fri, 07 Jun 2013 20:15:32 GMT. With a successful track record in both the CRO and resourcing fields, Ockham is driven by outcome, defined by expertise. For more information about Ockham, visit www.ockham.com . One of our clients is looking for a Project Director. This is a perm position. Acting as the first point of contact for the Project Managers and freelancers, the Project Director is responsible for ensuring that projects...

Project Director - Home Based

Location: Tampa Florida

Description: Ockham Development Group Inc is currently interviewing Project Director - Home Based right now, this vacancy will be placed in Florida. For detail informations about this vacancy opportunity kindly see the descriptions. With a successful track record in both the CRO and resourcing fields, Ockham is driven by outcome, defined by expertise. For more information about Ockham, visit www.ockham.co! m . One of our clients is looking for a Project Director. This is a perm position.

Acting as the first point of contact for the Project Managers and freelancers, the Project Director is responsible for ensuring that projects are resourced with suitably qualified and skilled staff and that the progress of project timelines are being met.

Main Tasks

  • To monitor the scope of work in the contract with the actual scope of work and to notify the VP Global Operations if additional tasks are needed in order to deliver on the project timeline and quality standards for all projects.
  • To assist with allocation of resource for projects.
  • To represent the Company at meetings with ongoing & potential clients.
  • To input into proposals for new projects including clinical team member allocation, budgets and feasibility for new studies.
  • To ensure, we are in an audit ready condition at all times.
  • To facilitate feasib! ility assessments.
  • To assist with identification and ! screening of potential candidates for project management roles.
  • To ensure Project Managers are trained and comply with all relevant SOPs and regulations.
  • To recommend additional training requirements of project team members to the VP Global Operations.
  • To conduct, as appropriate, grievance, disciplinary, performance/absence management interviews.
  • To make decisions regarding career progression and project team allocation for staff.
  • To meet with the VP Global Operations on a regular basis to keep update on project progress.
  • To provide project support and mentoring for project teams.
  • To conduct monthly project review meeting with Project Managers.
  • To attend project team meetings with sponsor on a regular basis in order to interface with the sponsor (teleconferences and face to face meetings).
  • To assist and contribute to performance reviews for Project Managers with input from colleagues (eg CRAs, ! CTAs and other members of the management team where necessary.
  • To review company procedures on an ongoing basis in order to ensure the highest standards of clinical research.
  • To remain up to date with all relevant SOPs and regulatory requirements.
Requirements

Experience working directly for a CRO and min 2 years of Oncology required.

Education Requirements

Bachelor’s degree or licensed certified health care training, or equivalent combination of education and experience.

Skills and Knowledge

  • Extensive knowledge of the conduct of clinical trials and the regulations and guidelines controlling their conduct.
  • Expertise in motivating and integrating project teams.
  • Expertise in providing senior oversight of projects and project teams.
  • Must possess leadership skills in an international environment and be customer service oriented.
  • Possess good interpersonal ski! lls, self-motivated and retain a positive attitude.
  • Good teach! ing and mentoring skills.
  • Knowledge of U.S. Food and Drug Administration (FDA), ICH, and Good Clinical Practice (GCP) guidelines.
  • The ability to oversee and supervise project managers and senior project managers.
Keywords: SAS, SAS Programmer, Statistics, Statistical Programmer, Statistical Analysis, ISS/ISE, Biostatistician, Biostatistical Programmer, Clinical Trials, Clinical Research, Clinical Studies, Pharmaceuticals, Drug Development, IND, NDA, Data Management, Data Manager, Clinical Data Manager, Clinical Data Coordinator, Drug Safety, Drug Safety Specialist, Drug Safety Associate, Pharmacovigilence, Drug Safety Nurse, Drug Safety Physician, Medical Writer, Medical Writing, Regulatory Affairs, Regulatory Submissions, Clinical Project Manager, Clinical Trials Specialist, Medical Services Specialist, BSN, RN, Clinical Research Associate, CRA, Clinical Study Manager, Clinical Study Monitor, Clinical Trials Monitoring, Regional CRA, Reg! ional Clinical Research Associate, In-house CRA, In-house Clinical Research Associate, CDISC, SDTM, ADaM, Rave, Medidata, InForm, Home based, telecommuting, ASG, Ockham
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If you were eligible to this vacancy, please email us your resume, with salary requirements and a resume to Ockham Development Group Inc.

If you interested on this vacancy just click on the Apply button, you will be redirected to the official website

This vacancy starts available on: Fri, 07 Jun 2013 20:15:32 GMT



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