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Clinical Research Asociate Resume

SUMMARY:

  • To secure a challenging position in Clinical Research especially where my skills and knowledge can be applied for a successful and satisfying career.
  • Wish to excel and upgrade myself at a pioneering institution which is involved in new discoveries and be a part of it for interdisciplinary exposure and to pursue knowledge which can be imparted for generations for their betterment and noble cause.
  • Knowledge of GCP and Confidential guidelines including basic understanding of regulatory requirements.
  • Basic and advanced knowledge of clinical trial process.

FIELD OF INTEREST:

  • Clinical Research Associate
  • Project Management
  • Pharmacovigilance
  • Clinical Data Management
  • R & D department
  • Quality Assurance.
  • Regulatory affairs.
  • Clinical Research Coordinator.

SKILLS:

  • Able to work in team and manage leadership.
  • Management skills.
  • Excellent interpersonal and communication skills.
  • Proficient with Microsoft Office

PROFESSIONAL EXPERIENCE:

Clinical Research Asociate

Confidential

Responsibilities:

  • Develop SOPs to evaluate clinical samples
  • Develop and perform assays on human clinical samples with accuracy consistency
  • Assistance in the coordination of domestic & international shipping for clinical sample, management and clinical sample storage
  • Utilize established mathematical programs and scientific techniques to compile analyze data
  • Record procedures, outcomes observations in lab notebook following established guidelines
  • Monitor laboratory supply inventories, compile supply lists for clinical trials
  • Present research at group meetings
  • Work closely with clinical research coordinators for future on - going clinical trials
  • Communicate with clinical collaborators about research management on regular basis
  • Carry out start up and close out study of clinical trials

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