长沙招聘

PURPOSE

Perform, manage and co-ordinate activities associated with feasibility for assigned opportunities/ projects. Collate data and present to internal stakeholders together with recommendations. Train and mentor junior staff.

 

RESPONSIBILITIES

？ Accountable for making recommendations for Quintiles commitments for future studies in terms of recruitment rate,

timelines and screen failure rates

？ Take independent responsibility for capability exercises and larger feasibility projects / deliverables

？ Prepare for strategy calls by research into therapeutic areas using internal databases, scientific literature, the internet and expert medical knowledge to provide background information.

？ Attend strategy calls with internal stakeholders including Medical Directors and Advisors, Business Developers, Sales Staff and Program Directors. Present background information, particularly including country recruitment and screen failure data.

？ Design of protocol-specific questionnaires for collection of global feasibility information for individual countries and sites in order to determine patient populations and protocol suitability.

？ Develop feasibility analysis systems and data collection tools in Excel to support the collection of associated metrics

？ Provide appropriate tools for country feasibility leads to carry out feasibility and capability exercises e.g. telephone training and detailed emails

？ Coordinate the collection and analysis of global feasibility information to meet the challenging timelines of the proposal process and independent feasibility assessments

？ Reconcile and interpret feasibility data, providing solid recommendations to internal stakeholders

？ Production of feasibility text for proposals and feasibility reports

？ Review budgets for stand-alone paid feasibility studies

？ Train and support new team members

？ Attend client meetings as required to present feasibility process and explain recommendations

？ Liaise with internal and external customers globally to coordinate the collection and delivery of feasibility data.

？ Maintain and update departmental information repositories and databases

？ Undertake therapeutic training, as necessary, and keep abreast of developments in clinical research generally

All responsibilities are essential job functions unless noted as nonessential (N).

 

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

？ Clinical/project management experience is preferred.

？ General knowledge and understanding of company clinical systems, procedures and corporate standards.

？ Good knowledge of medical terminology, GCP, FDA regulations, and Drug Development process.

？ In-depth understanding of clinical research.

？ Excellent communication, organizational and interpersonal skills.

？ Fluid report writing in English

？ Strong computer literacy, including well-developed computer skills in applicable software.

？ Ability to work independently and effectively prioritize tasks.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

？ Bachelor’s Degree in Healthcare or Biological Science and a minimum of 3 years related experience in clinical research; or equivalent combination of education, training and experience

 

PHYSICAL REQUIREMENTS

？ Extensive use of keyboard requiring repetitive motion of fingers.

？ Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

？ Regular sitting for extended periods of time.

？ May require occasional travel.

QuintilesIMS pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster.
 
If that is your passion, we have a place for you.