Precision Medicine Group

More roles at Precision Medicine Group

Clinical Trial Manager

Region Restricted

Remote work allowed only within certain countries or regions.

Employer listed it 5 days ago · Added 4 weeks ago

Been open since 4 weeks ago, still being checked, but it has been live a while.

Salary

Not stated

Location

Timezone

CET ±2

Contract

Full-time

Experience

Mid

What the advert says

Quoted word for word from the employer's advert. Where it says nothing, we say so.

Working hours: Not mentioned in the advert
Where you can work from: Candidates must be legally authorized to work in the country of employment without employer sponsorship.
Contract: Not mentioned in the advert
Experience asked for: Not mentioned in the advert
Pay: Not mentioned in the advert

Remote flexibility

Region Restricted

Remote work is allowed, but only for candidates based in Poland, Slovakia.

What the employer says

Source listing states candidate location: "Remote, Poland, Slovakia (Bratislava)"
Job description states: "authorized to work in the country of employment without"

What Nomaders makes of it

Timezone overlap with the listed area is often expected

The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.

Before you apply

Questions worth asking: Nomaders interpretation

No pay is stated. Ask for the salary range before investing time in interviews.
The advert does not say whether this is employment or a contractor arrangement. Ask, as it affects tax and benefits.

Produced automatically from this advert's text; not reviewed by a person. The employer's own page is the final word.

About the role

Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in Hungary, Poland, Romania, Serbia or Slovakia.

Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.

You will be the hub of central intelligence for the studies you will be managing and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.

We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.

About You:

You love having responsibility and a say in how clinical trials are run

You plan ahead, but have alternative options and a flexible approach

You are client focused

You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.

You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly

You are a master at identifying any risks that threaten projects and handle them resolutely

You thrive and work with autonomy and ownership to deliver successful outcomes

The day-to-day role, and how we will support your continued growth:

Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out

Successful execution of assigned trials and ensuring completion of trial deliverables

Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members

Mentoring and training of team members

Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor

Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities

Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction

Qualifications:

Minimum Required:

Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology

Other Required:

Requirements

·You love having responsibility and a say in how clinical trials are run
·You plan ahead, but have alternative options and a flexible approach
·You are client focused
·You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.
·You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly

Benefits

No benefits package published with this listing. Ask about it at first interview.

How to apply

1Check the flexibility label above, region restricted, matches where you plan to live and work.
2Tailor your CV to the role at Precision Medicine Group, mentioning your remote working experience and working hours (CET ±2).
3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.

Found 27d ago. Last checked today. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.