Clinical research associate Work, Jobs in Witney (with Salaries)

Site Management Associate I
PSI CRO —Oxford
- Full-time
- Hybrid work
- Bachelor's degree
- Organisational skills
Quick apply
Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays
Moderna, Inc. —Oxford
- Full-time
- Bachelor's degree
- Communication skills
- Annual leave

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Senior Research Associate, Bioanalytical & Molecular Assays
Moderna, Inc. —Oxford
This role sits at the intersection of basic science research, bioanalysis, and clinical development, helping advance innovative mRNA programs through phase-…
Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays
Moderna, Inc. —Oxford
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Here's What You'll Do:

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Site Management Associate I

PSI CRO -
Oxford

Quick apply

Job details

Full-time

Qualifications

Document control
Meeting coordination
Clinical research
Filing
Internal department liaison
Microsoft Office Suite
Bachelor's degree
Organisational skills
Document management

Full job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Based in Oxford - Hybrid 2 days in office

Job Description

Join our international team and be the key support to clinical research projects in the UK, streamlining communication, maintaining systems and managing documents & information.

Site Management

Exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team
Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies
Assists with handling administrative financial tasks
Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections

Other Communication

Exchanges data, documents, and other information with the project team and other departments
Provides assistance with organization of internal team meetings
Prepares draft minutes of internal team meetings
Assists with preparation, attendance and follow-up of Investigator’s Meetings, as applicable
Under supervision, maintains study-specific and corporate tracking systems

Document Management

Maintains Trial Master File (TMF)
Perform TMF review and oversight at country and site level
Prepares, distributes, and updates Onsite Study Files (OSF) and OSF checklists
Provides assistance with translations

Safety Management

Ensures proper safety information flow with investigative sites

Other Assistance

Provides miscellaneous administrative project support (if applicable)

Qualifications

College/University Degree in Life Sciences
Experience in Clinical Research / CRO environment, preferably in an international setting, is a plus
Prior experience of work as a Site Coordinator is a plus
Proficiency in standard MS Office applications
Good organizational and planning skills, problem-solving abilities, flexibility
Detail-oriented, able to multi-task and work effectively in a fast-paced environment
Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.

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clinical research associate jobs in witney

Site Management Associate I

Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

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