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Clinical Trial Investigators - Pis & Sub-Is (Pte Or Fte)

Buscojobs

Greater London

On-site

GBP 30,000 - 60,000

4 days ago

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An innovative clinical trial unit is seeking Clinical Trial Investigators to provide medical support for various trials. This position offers a unique opportunity to work with state-of-the-art facilities and contribute to the growth of a newly established organization. The ideal candidate will possess a medical degree and experience as a Sub-Investigator or Principal Investigator, showcasing their entrepreneurial spirit. Join a collaborative team that values low staff turnover and offers ample opportunities for professional growth. If you're passionate about advancing clinical research and making a difference in patient care, this role is perfect for you.

Room for growth and development

Collaborative culture

Salary package (Base, Super, Annual Leave)

Extra paid leave

Free onsite parking

Qualified medical doctor with full AHPRA registration is essential.
Prior experience as a Sub-I or PI is necessary for this role.

Understand study protocols and educate patients on trials.
Supervise investigators' activities and ensure compliance with regulations.
Engage with sponsors for protocol amendments.

AHPRA registration

Experience as Sub-I or PI

Teamwork

Communication with patients

Organisational skills

Attention to detail

Work on Phase I-III clinical studies

Qualified medical doctor

Clinical Trial Investigators - PIs & Sub-Is (PTE or FTE)

3 days ago Be among the first 25 applicants

Direct message the job poster from Tardis Group

About the Organisation and the Position

The company is a clinical trial unit that delivers high standard quality services across a wide range of therapeutic areas. With state-of-the-art equipment and facilities, the organisation is committed to becoming one of the best early-phase clinical trial service providers in the country.

The aim of the position is to provide medical support for the conduct of clinical trials, in accordance with quality standards, SOPs and adequate regulations and guidelines. The right applicant will be an experienced Sub-I or PI willing to use their entrepreneurial spirit to help grow a newly established organisation.

Responsibilities

Understanding of study protocol, investigator’s brochure and informed consent form (ICF)
Assessing patient condition with physical examination and medical history
Reviewing clinical pathology reports, vital signs and ECG reports
Educating patients on trials
Supervising all investigators' activities relating to the clinical trial (PI specific)
Having ultimate responsibility for the conduct of studies (PI specific)
Being contactable by research staff (PI specific)
Signing off on all training of all research staff working on the clinical trial (PI specific)
Engaging with sponsors regarding necessary protocol amendments (PI specific)

Skills and Experience

Qualified medical doctor with full AHPRA registration
Prior experience as a Sub-I or PI is necessary
Ability to work well in a team and communicate with patients
Solid organisational skills
High attention to details
Must be a citizen / PR of Australia / New Zealand
Work on Phase I-III clinical studies

Benefits

Plenty of room to grow and develop as part of a fast-growing organisation
Highly positive and collaborative culture which has resulted in very low staff turnover
Salary package (Base, Super, Annual Leave, etc.)
1 extra day of paid leave / month
Free onsite parking

For More Details

Please contact Chris at

Seniority Level: Mid-Senior level

Employment Type: Part-time

Job Function: Research and Health Care Provider

Research Services: Biotechnology Research, and Pharmaceutical Manufacturing

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