Clinical Trial Assistant (Hybrid / Luton)

Clinical Trial Assistant (Hybrid / Luton)

19 Oct
|
Lifelancer
|
Reading

19 Oct

Lifelancer

Reading

Job description

Our sponsor dedicated (cFSP) team are seeking a CTA to join us on our mission to drive healthcare forward.

Hybrid working on offer, with 2-3 days per week required on-site in Luton with the sponsor; a global biopharmaceutical.

The CTA will perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

Essential Functions

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.

g., Trial Master File (TMF)) that track site compliance and performance within project timelines.







Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.

Assist with periodic review of study files and completeness.

Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

Act as a mentor for less experienced Clinical Trial Assistants (CTAs).

Assist with training and onboarding of new CTAs.

May serve as subject matter expert for business processes.

May lead CTA study teams.

May assist with interviewing and screening of potential new team members

May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.







May participate in departmental quality or process improvement initiatives.

Qualifications

Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)

Minimum 6 months clinical research experience strongly preferred.

Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.

Effective written and verbal communication skills including good command of English language.

Effective time management and organizational skills.

Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Lifelancer ( https : / / lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT.





The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https : / / lifelancer.com / jobs / view / 390425373e797e3c12d65a36122f7b81

▶️ Clinical Trial Assistant (Hybrid / Luton)
🖊️ Lifelancer
📍 Reading

Subscribe to this job alert:
Enter Your E-mail address to receive the latest job offers for: clinical trial assistant (hybrid / luton)

Clinical Trial Assistant (Hybrid / Luton)

Clinical Trial Assistant (Hybrid / Luton)

Job description Our sponsor dedicated (cFSP) team are seeking a CTA to join us on our mission to drive healthcare forward. Hybrid working on offer, with 2-3 days per week required on-site in Luton with the sponsor; a global biopharmaceutical. The [...]
Reading
19 Oct
    Reading
    19 Oct

Clinical Trial Coordinator

Clinical Trial Coordinator

Job Details Job Overview Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and / or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), an [...]
Reading
19 Aug
    Reading
    19 Aug

Clinical Trials Assistant

Clinical Trials Assistant

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Researc [...]
Reading
16 Oct
    Reading
    16 Oct

Clinical Project Manager

Clinical Project Manager

Job description Clinical Project Manager Sponsor Dedicated, Home Based, UK Join us on our exciting journey! Remote / Hybrid / Office based working options. Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare [...]
Reading
31 Oct
    Reading
    31 Oct
Subscribe to this job alert:
Enter Your E-mail address to receive the latest job offers for: clinical trial assistant (hybrid / luton)