Back to Job SearchWe are currently looking for an Associate Clinical Project Manager to join a leading life sciences company based in the Berkshire area. As the Associate Clinical Project Manager, you will be responsible for providing hands-on operational support to a Clinical Project Manager to deliver clinical studies from protocol through final report and archiving of the trial master file.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Associate Clinical Project Manager will be varied; however, the key duties and responsibilities are as follows:
1. As the Associate Clinical Project Manager, you will keep the trial master file complete and ready for audit or inspection through routine reviews and follow-up with document owners.
2. As the Associate Clinical Project Manager, you will support the creation, review, and finalisation of study documents, including protocols, amendments, consent forms, plans, submissions, and study reports.
3. As the Associate Clinical Project Manager, you will coordinate stakeholder communication, meetings, decisions, and action logs, and maintain accurate study contact lists and procedure references.
4. As the Associate Clinical Project Manager, you will track study status, metrics, invoices, and risks, and share clear updates with the study team and leadership.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Associate Clinical Project Manager, we are looking to identify the following on your profile and past history:
1. Bachelor’s degree (or equivalent) in a relevant scientific, health, or business discipline.
2. Proven industry experience in clinical research, such as monitoring, trial coordination, or project support.
3. A working knowledge and practical experience with office productivity tools and study systems, with strong attention to detail and data quality.
Key Words: Associate Clinical Project Manager / Clinical Research / Clinical Studies / Trial Coordination / Clinical Project Support / Life Sciences / Clinical Operations / Study Documentation / Clinical Systems / Regulatory Requirements / Pharma / Pharmaceutical / Biopharma / CRO / clinical / project / coordination / systems / trial / documentation / audit / compliance / communication / healthcare / research / pharmaceutical / regulatory / support / #LI-DNI
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Associate Clinical Project Manager will be varied; however, the key duties and responsibilities are as follows:
1. As the Associate Clinical Project Manager, you will keep the trial master file complete and ready for audit or inspection through routine reviews and follow-up with document owners.
2. As the Associate Clinical Project Manager, you will support the creation, review, and finalisation of study documents, including protocols, amendments, consent forms, plans, submissions, and study reports.
3. As the Associate Clinical Project Manager, you will coordinate stakeholder communication, meetings, decisions, and action logs, and maintain accurate study contact lists and procedure references.
4. As the Associate Clinical Project Manager, you will track study status, metrics, invoices, and risks, and share clear updates with the study team and leadership.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Associate Clinical Project Manager, we are looking to identify the following on your profile and past history:
1. Bachelor’s degree (or equivalent) in a relevant scientific, health, or business discipline.
2. Proven industry experience in clinical research, such as monitoring, trial coordination, or project support.
3. A working knowledge and practical experience with office productivity tools and study systems, with strong attention to detail and data quality.
Key Words: Associate Clinical Project Manager / Clinical Research / Clinical Studies / Trial Coordination / Clinical Project Support / Life Sciences / Clinical Operations / Study Documentation / Clinical Systems / Regulatory Requirements / Pharma / Pharmaceutical / Biopharma / CRO / clinical / project / coordination / systems / trial / documentation / audit / compliance / communication / healthcare / research / pharmaceutical / regulatory / support / #LI-DNI
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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