Clinical Scientist - Operations - Signant Health | New Day Jobs (Yangon, Myanmar)

Easy Apply (Signant Health) Clinical Scientist - Operations job. View job description, responsibilities and qualifications. See if you qualify!

Signant Health
Remote (Asia Time Zone Permitted)

Clinical Scientist - Operations

Apply from Source

Clinical Scientist - Operations

Signant Health
Salary : Login to view salary Apply from Source
Job Type : Full-Time
Education Requirement : Bachelor Degree
Skills :
Experience : 3 to 5 years
Work Days : Monday To Friday
Share this
Job Detail

Signant Health is a global evidence generation company that helps companies digitally enable clinical trials. No matter how or where customers run their trials. We make the patient journey more natural and intuitive, and the data journey more direct and objective. Working at Signant Health puts you in the very heart of the world’s most exciting sector — a high-growth, dynamic company in an extraordinary industry. We are radically changing the clinical trial landscape, driving change through the technology and innovations we create and the services we deliver to our customers.

So, are you ready for the best work of your life?

Signant Health is currently recruiting for a new Clinical Scientist remote opportunity. In this role you are responsible for delivery of clinical trial projects and development of clinical products/services including training, endpoint reliability, and data analytics. This role will work collaboratively with internal /sponsor teams to define and build training for endpoint methodologies. In addition, this position will provide study materials and directly participate in presentations, virtual training, and face-to-face interactions . The Clinical Scientist is responsible for evaluating data according to approved methodologies and presenting reports as well as action plans to the sponsor. You will work with development teams to design, build and test eCOA needs for their projects and for potential opportunities.

Essential Duties And Responsibilities

Other duties may be assigned as needed

  • Attends internal and external project meetings (e.g., weekly external client call, Investigators’ Meetings)
  • Reviews protocol/CRF and provides feedback as appropriate
  • Contributes to the design and definition of project specific processes and data review methodologies
  • Develops clinical content (e.g., qualification methodologies, didactic presentations) for rater training and qualification programs for study staff in clinical trials
  • Ensures that patient and educational videos are developed in accordance with study specific sponsor requirements and conducts patient interviews, as appropriate
  • Evaluates data submitted in accordance with Endpoint Reliability programs and contacts raters, as appropriate, to gather additional information and provide feedback
  • Ensures that project clinical deliverables follow quality control standards
  • Proactively identifies and escalates potential project issues appropriately to project team, sponsor and/or manager
  • Communicates with study site staff in accordance with project specific methodology/SOPs and documents interaction in the respective IT application
  • Ensures compliance with quality assurance as outlined in SOPs/Clinical Operations Guidelines
  • Ensures consistency of product with actual project scope and resolves ambiguities in collaboration with both internal and external project teams
  • Assists in training, development, and retention of external Clinical Experts
  • Experience administering rating scales

Administration

  • Submits weekly report of activity to manager
  • Participates in orientation and training of staff as appropriate
  • Participates on committees as assigned
  • Completes required trainings in a timely manner
  • Enhances Signant Health Client Services business model by institutionalizing business processes, implementing best practices, templates, and seeking ways to work more efficiently
  • Ability to perform all responsibilities of Clinical Specialist, as required

Education

  • Master’s Degree, M.D., Ph.D., Psy.D, Pharm.D., in healthcare-related field, with one year of clinical experience, which includes administration of psychiatric and/or cognitive scales OR
  • Bachelor’s Degree or RN with 2 years of clinical experience, which includes administration of psychiatric and/or cognitive scales
  • Minimum of one year as successful Clinical Specialist

Personal Attributes

  • Excellent writing skills
  • Demonstrated strong analytical, organizational, creative problem solving and communication skills
  • Ability to succeed in a fast-paced, entrepreneurial environment
  • Basic knowledge of statistics
  • Competency conducting patient interviews
  • Comfortable with being on video
  • Competency working with data and numbers
  • Good negotiation and diplomacy skills
  • Successfully manages own time, proactively identifies, and prioritizes multiple tasks
  • Ability to work with staff at all levels and across various disciplines
  • Excellent computer skills including Word, Excel and PowerPoint
  • Fluency in English (will be required to write, speak and understand English to conduct day-to-day business)
  • Very detail oriented
  • Willingness to maintain flexible schedule

At Signant Health, accepting difference isn’t enough—we celebrate it, we support it, and we nurture it for the benefit of our team members, our clients and our community. Signant Health is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or veteran status.

Apply Now

Similar Jobs
LinkedIn-PH - 2 months ago
60 total views, 1 today
Similar Jobs
You will receive the email for your email confirmation. Please check!