STUDY START UP REGULATORY jobs in EUROPE ENGLAND, United Kingdom #2

, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase... visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team...

IQVIA

study start-up and clinical trial management processes at Medpace. The Site Contract Specialist will advance the start-up... with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations...

Medpace

department managers, ensuring compliance with all Legal & lender regulatory requirements, responsibility of offshore PC team... activities comply with Legal requirements, regulatory standards, and company policies Stay updated with changes in Conveyancing...

G2 Legal

, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents... findings and action plans by submitting regular visit reports, generating follow-up letters and other required study...

IQVIA

) Contract: Permanent Benefits: Pension; up to 26 days holiday (plus an additional two days at Christmas for office closure...); training and development opportunities; contribution to further studies and study leave allowance. Closing date: Friday 19th...

NFP People

advancements, regulatory changes, and macroeconomic factors. SWOT Analysis: Evaluate the Strengths, Weaknesses, Opportunities..., and Threats related to a specific market or company. Competitor Analysis: Study competitors market positions, product offerings...

Graduate Financial Recruitment

trial from start-up to closeout. 8. Excellent IT skills in the following areas: word processing, communication software, R... a large scale experiment or clinical trail from start up to close out that involved supervising a team to deliver high quality...

King's College London

for external training, interest-free travel loan scheme, discounted gym memberships, and Role Type: Full-time, permanent Start... Date: We are currently recruiting for start dates throughout 2024, including August and September, and you will be asked to state...

Costello Medical

to a range of other dissemination activities, as well as the set-up, running and closure of the large-scale clinical study. The successful candidate... of conducting a large-scale experiment and or clinical trial from start-up to closeout. 8. Excellent IT skills in the following...

King's College London

all operational aspects for implementation and conduct of global clinical trial activities from study start-up to CSR, in respect... study for: insurance certificate, contracts signature process, set-up and management of the Trial Master File (eTMF...

Ipsen

-free travel loan scheme, discounted gym memberships, and Role Type: Full-time, permanent Start Date: We are currently... recruiting for start dates throughout 2024, including August and September, and you will be asked to state your availability...

Costello Medical

George Higginson is currently searching for an experienced Safety Scientist. He is partnering with an up-and-coming..., participate in monitoring, review, analyses, interpretation and evaluation of incoming safety information (instream clinical study...

AL Solutions

query generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents... findings and action plans by submitting regular visit reports, generating follow-up letters and other required study...

IQVIA

and knowledge that sets up the best start to your career. We offer competitive entry salaries from £14,000 to £20,500pa and fully... and have a warm welcome from day 1. There is a member of our Apprentice team at each site, helping you progress, ensuring your study...

Leonardo

and resolution. May support start-up phase Ensure copies/originals (as required) site documents are available for filing in the... and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation...

IQVIA

for their lead candidate to start clinical trials. This will be a hybrid role requiring you to be on-site in Oxford at least once.... Contribution to the development and review of regulatory submissions and interaction with Regulatory Authorities. Oversight of the...

CK Group

650 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services... and how to work changes in regulatory landscape, new technologies like artificial intelligence, machine learning, predictive pricing...

EVERSANA