Intermediate (2-5 years of experience)
Summary of the Role
As a Clinical Pharmacologist, the successful candidate will be instrumental in the design, implementation, and analysis of drug studies in humans. This position involves working closely with cross-functional teams to evaluate the safety and efficacy of new medications. The role requires an understanding of pharmacokinetics, pharmacodynamics, and drug metabolism, as well as strong analytical skills to interpret clinical data.
Required Skills
Expertise in clinical study design and execution.
Proficiency in data analysis and statistical methods.
Strong knowledge of pharmacokinetics, pharmacodynamics, and drug metabolism.
Excellent communication and presentation skills.
Critical thinking and problem-solving abilities in complex clinical research scenarios.
Proficiency with clinical trial software and statistical packages such as SAS or R.
Ability to interpret and adhere to regulatory guidelines and ethical standards.
Qualifications
Doctorate degree in pharmacology, pharmacy, medicine, or a related field.
Minimum of 2 years of experience in clinical pharmacology or a similar role within the pharmaceutical industry.
Proven track record of designing and conducting clinical pharmacology studies.
Strong working knowledge of regulatory requirements pertaining to clinical pharmacology.
Experience with pharmacokinetic and pharmacodynamic modeling is highly desirable.
Familiarity with bioanalytical method development and validation.
Ability to work in a fast-paced, interdisciplinary environment with excellent team collaboration skills.
Responsibilities
Design and conduct clinical pharmacology studies to analyze the safety, efficacy, and pharmacokinetics of new drugs.
Collaborate with cross-disciplinary teams including researchers, statisticians, and clinical operations to ensure study success.
Contribute to the development of clinical trial protocols, including the selection of appropriate doses and dosing regimens.
Provide expert analysis of clinical pharmacology data and contribute to the preparation of regulatory submission documents.
Monitor emerging trends and advancements in clinical pharmacology and drug development.
Ensure compliance with ethical, legal, and regulatory standards during the conduct of clinical trials.
Participate in the preparation of manuscripts and presentations for scientific meetings and publications.