Clinical pharmacology jobs in RichmondCreate job alerts

In-depth knowledge of clinical pharmacology, PK/PD , and clinical data interpretation. The ideal candidate will have a strong background in clinical pharmacology, pharmacokinetics (PK), and pharmacodynamics (PD), with the ability to critically evaluate and interpret data and manage clinical trial...

The Medical Director, Clinical Pharmacology (MD CP) will be the primary point of contact for the cross-functional Clinical Pharmacology (CP) Trial Team and for our qualified CROs used in the Clinical Pharmacology Partnership Model for any safety-related, medical and clinical pharmacology-related ...

Serve as the Clinical Pharmacology lead, providing expert guidance and support to clinical-stage project teams. * Lead the analysis, interpretation, integration, and reporting of clinical ...

Have an expert understanding of the different approaches related to nonclinical pharmacokinetics * Apply understanding of physical properties, DMPK and enzymology to contribute to the design of new ...

Pharmacovigilance Manager Upward Reporting: Head of Quality and Drug Safety Position Type ... Review and manage updates to Risk Management Plans, including liaising with clinical colleagues on ...

Ability to plan, organise and follow up * Track and plan clinical activities to meet agreed timelines * Maintain a current awareness of pharmacovigilance requirements * Effective verbal and written ...

Provide pharmacovigilance oversight for clinical trials, post-market surveillance, and expanded access programs, ensuring integration of safety data * Perform peer review of cases in safety databases ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Strategic leadership of pharmacovigilance, medical writing and laboratory data management services. * Full P&L responsibility for non clinical services. * Lead and deliver business development ...

Proven experience in medical monitoring, pharmacovigilance, and drug safety within a CRO, pharmaceutical, or clinical trial setting. * Clinical Trial Expertise: A strong grasp of clinical trial ...

Biotrial is a leading CRO specializing in Drug Development with a wide range of expertise in preclinical pharmacology, clinical development, bioanalysis, biometrics and ECG, CNS and Imaging Core Lab

Act as the scientific lead liaising with key stakeholders (e.g., PIs, KOLs, DMCs, Pharmacovigilance, Biometrics), ensuring effective study execution and compliance with Good Clinical Practice (GCP

Strong background in clinical development or pharmacovigilance, ideally in rare diseases. * Experience with regulatory submissions (FDA/EMA) or working within regulatory agencies. If this role is for ...

... Clinical Trials, Non-interventional Studies, Patient Oriented Program (POPs), Literature ... Knowledge of national and international regulations for pharmacovigilance Knowledge of ...

We have extensive functional expertise including Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

... Clinical Trials, Non-interventional Studies, Patient Oriented Program (POPs), Literature ... Skills & Knowledge: • Knowledge of national and international regulations for pharmacovigilance ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...