Associate Clinical

Key Responsibilities

• Lead clinical studies involving

  healthy volunteers and patient populations

  , ensuring effective organization and prioritization of tasks.
• Own and be accountable for all

  Data Management (DM) deliverables

  , providing guidance to the DM team to maintain high-quality standards.
• Ensure adherence to

  protocols

  ,

  global SOPs

  , and

  Good Clinical Practice (GCP)

  standards across projects.
• Collaborate with

  Project Managers

  to define study timelines and maintain communication with cross-functional leads throughout the project lifecycle.
• Provide

  leadership

  to DM project teams, coordinating internal meetings and collaborating with

  EDC Design

  ,

  SAS Programming

  , and

  Statistics

  teams.
• Monitor project risks, develop

  mitigation strategies

  , and use

  data-driven insights

  to meet

  database lock timelines

  .
• Keep stakeholders informed on

  budget status

  ,

  scope changes

  , and

  timeline impacts

  .
• Build and maintain

  strong client relationships

  , incorporating feedback from

  client satisfaction surveys

  to enhance service quality.
• Track and document

  scope changes

  , ensuring appropriate approvals are obtained.

• Mentor and coach

  internal teams on DM processes, best practices, and continuous improvement.
• Support DM managers in

  team performance evaluations

  and provide

  constructive feedback

  .
• Stay current with

  emerging DM technologies

  and

  industry trends

  to drive innovation.
• Maintain accurate records of all data management work and reconcile

  clinical databases

  with

  safety

  and

  lab data

  .
• Represent DM and

  Biometrics

  in

  business development activities

  , including audits and sponsor meetings.
• Promote Biometrics services to sponsors and perform

  additional responsibilities

  as needed.

Qualifications

Education

• University/college degree required;

  equivalent relevant experience

  may be considered in lieu of formal education.

Experience

• 68 years of v experience

  , with at least

  1 year of direct sponsor/client management

  .
• Experience in

  scope management

  ,

  budget tracking

  , and

  handling client concerns

  is preferred.
• Strong understanding of the

  clinical trial process

  , including DM, clinical operations, and biometrics.
• Proven ability to meet

  project timelines

  with excellent

  time management

  and

  organizational skills

  .
• Strong

  interpersonal

  and

  communication

  skills; ability to work collaboratively in a

  team environment

  .
• Familiarity with

  medical terminology

  .