Clinical Consultant Specialist Science & Medicine

South Africa, South Africa

Job Description


Are you ready for the Most Impactful Work of Your Life?Signant Health is a global evidence-generation company. Were helping our customers digitally enable their clinical trial programs, meeting patients where they are, driving change through technology and innovations, and reimagining the path to proof.Working at Signant Health puts you in the very heart of the worlds most exciting sector - a high-growth, dynamic company in an extraordinary industryWhere do you fit in?The Clinical Consultant Specialist provides support to supervisor and is responsible for delegated services/tasks to deliver defined requirements and meet company strategic objectives. The Clinical Consultant Specialist participates in applicable aspects in the identification, vetting, training and calibrations, and invoicing and payment of clinical consultants. The Clinical Consultant Specialist also has responsibility for maintenance and classification of consultant information and materials. The Clinical Consultant Specialist provides input toward process improvement based on experience and may have additional duties as assigned.Want to join the Best Team of Your Life?Were looking for people who are excited by the potential to make a difference in the world. You dont need to have a clinical background to thrive at Signant. You need to be decisive, open to celebrating mistakes, able to communicate transparently and inclusively, and someone your team can count on. Most of all you need to be yourself!As part of our team, your main responsibilities will:

  • Conducts all activities in full accordance to Good Clinical Practice guidelines.
  • Works closely with supervisor to identify clinical consultants for US and global projects.
  • Pulls database reports and identifies potential candidates.
  • Contacts possible consulting candidates and gathers, tracks, and maintains necessary information.
  • Works with clinical staff to vet and obtain approval of consultants.
  • Maintains database and other records of clinical consultant information, credentials, etc.
  • Reviews clinical consultant monthly invoices.
  • Works with finance and accounting to track payment of clinical consultants.
  • Assigns and tracks completion of general training and calibration exercises.
  • May assign work to clinical consultants as directed.
DECISION MAKING AND INFLUENCE
  • Conducts all activities in full accordance to Good Clinical Practice guidelines.
  • Works closely with supervisor to identify clinical consultants for US and global projects.
  • Pulls database reports and identifies potential candidates.
  • Contacts possible consulting candidates and gathers, tracks, and maintains necessary information.
  • Works with clinical staff to vet and obtain approval of consultants.
  • Maintains database and other records of clinical consultant information, credentials, etc.
  • Reviews clinical consultant monthly invoices.
  • Works with finance and accounting to track payment of clinical consultants.
  • Assigns and tracks completion of general training and calibration exercises.
  • May assign work to clinical consultants as directed.
Youll need to bring:Essential:
  • Bachelors degree or equivalent OR Associate Degree OR HS Diploma with relevant experience.
  • Must have excellent time management, communication (oral and written), and organizational skills.
  • Must have MS Office Suite experience Word, Excel, PowerPoint.
  • Able to multi-task and work with multiple cross-functional teams.
  • Must be able to communicate and engage effectively and have excellent written and spoken English skills.
  • Must be comfortable working with individuals from diverse countries, languages, and cultures.
  • Must be detail oriented.
  • Must show initiative and be able to work independently as needed.
Desirable:
  • Project Management experience OR equivalent.
  • Experience of clinical trials/pharmaceutical industry/life sciences.
  • Background in Pharmaceutical, Medical education and/or CRO.
  • Experience/understanding of the clinical research environment and GCP principles is preferred.
  • Competency working in custom data bases and excel reporting.
Does this sound like youd like to explore? Then wed love to hear from you!Please apply below.
We review and respond to every application, keep an eye on your inbox for our reply.Please note that Signant does not accept unsolicited resumes from Third Party vendors.#LI-CL1At Signant Health, accepting difference isnt 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.

Signant Health

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Job Detail

  • Job Id
    JD1377026
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    South Africa, South Africa
  • Education
    Not mentioned