EMPREGO CLINICAL TRIAL RISK BASED

Description clinical trial supplies manager ** emea based ** syneos health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...

Description clinical trial supplies manager syneos health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success...

Candidate must have clinical document qc experience (eg, clinical protocols, clinical study reports, investigator’s brochures)... the clinical editor will copyedit/proofread...

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our...

Years clinical research experience... knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

Reconciles contents of the isf with the trial master file (tmf)...  participates in global clinical monitoring/project staff meetings (inclusive of sponsor representation...

Knowledge of regulatory requirements and ethical guidelines pertaining to clinical research... the ideal candidate will have a proven track record of conducting...

This role can be conducted either office based / hybrid / home based in south africa - the choice is yours... associate medical safety director role responsibilities:...

Associate medical safety director role responsibilities: providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s...

Our mission is to innovate and deliver comprehensive solutions that improve clinical trial processes and patient care... qualifications: proven experience in a senior...

Required knowledge, skills, and abilities knowledge of clinical trial conduct at clinical study sites for pharmaceutical research... no certification required; preferred:...

Knowledge of clinical trial conduct at clinical study sites for pharmaceutical research... no certification required; preferred: "ccrc"- certified clinical research...

•    extensive experience in a cro/pharmaceutical industry and related clinical trial expertise (study coordinator, cra, pharmacy, nursing, healthcare administration)...

Strong knowledge of good clinical practice/ich guidelines and other applicable regulatory requirements, i... lead and ensure consistency in contingency planning...

Independent sae/susar management (submissions, unblinding, clinical trial reconciliations)   preparation of database outputs for periodic reporting (pbrer, dsur...

·        knowledge of good clinical practice/ich guidelines and other applicable regulatory requirements...   job responsibilities   ·        reviews and interrogates...