Sr. CTM Associate

Kite Pharma; Greater London; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading biopharmaceutical company in Greater London is seeking a Clinical Research Associate to conduct site evaluations and ensure compliance with regulations. The ideal candidate will have significant experience in clinical research, strong communication skills, and a bachelor’s degree in a scientific discipline. This position offers a full-time opportunity with emphasis on teamwork and personal development.

Qualifications

• 4 years of experience in clinical research or a related field.
• Ability to prioritize multiple tasks and plan proactively.
• Must have knowledge of FDA and EMEA regulations.

Responsibilities

• Conduct site evaluations, initiations, and closeout visits.
• Ensure site compliance with protocol and regulatory requirements.
• Assist in setting study timelines and CRO/vendor selection.

Skills

Excellent verbal and written communication

Interpersonal skills

Presentation skills

Data analysis

Education

Bachelor's degree in a relevant scientific discipline

RN certification

CCRA or other certification

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Job description

Job Description

Were here for one reason and one reason only to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. Weve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But were not finished yet.

Join Kite as we make even bigger advances in cancer therapies and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future you are the key driver in evolving our culture and creating an environment where every employee feels included developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Education & Experience Requirements

• 4 years of experience and a BS or BA in a relevant scientific discipline.
• 4 years of experience and an RN (2 or 3 year certificate).
• CCRA or other certification desired.

Job Responsibilities

• Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas. With limited supervision conducts site evaluations / initiations and closeout visits in addition to routine monitoring visits as required.
• Assures site compliance with the routine protocol and regulatory requirements and quality of data.
• Assists in the setting and updating of study timelines.
• Assists in CRO or vendor selection.
• With guidance from supervisor coordinates CROs or vendors.
• Drafts and coordinates review of protocols informed consents case report forms and monitoring plans.
• Assists in the review of routine data and preparation of safety interim and final study reports and resolution of data discrepancies.
• Participates or effectively runs meetings and conference calls with CROs vendors and multi-functional teams.
• May participate in abstract presentations oral presentations and manuscript development. Interfaces with individuals in other functional areas to address routine study issues.
• May be asked to assist in the training of Clinical Research Associates and Clinical Project Assistants.
• Under general supervision participates in two or more departmental or interdepartmental strategic initiatives.
• Travel is required.
• Excellent verbal written interpersonal and presentation skills are required.
• Working knowledge and experience with Word PowerPoint and Excel. Working knowledge of FDA and / or EMEA Regulations ICH Guidelines and GCPs governing the conduct of routine clinical trials.
• Must be able to prioritize multiple tasks plan proactively and accomplish goals using well-defined instructions and procedures.
• Ability to develop tools and processes that increase measured efficiencies of the project.
• Must be able to anticipate obstacles and proactively develop solutions to achieve project goals.
• Must have a general understanding of functional issues and routine project goals from an organizational perspective.

Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune systems ability to recognize and kill tumors. Kite is based in Santa Monica CA. For more information on Kite please visit . Sign up to follow @KitePharma on Twitter at Employment Opportunity (EEO)

is the policy of Gilead Sciences Inc. and its subsidiaries and affiliates (collectively Gilead or the Company) to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable all employment actions relating to issues such as compensation benefits transfers layoffs. returns from layoffs company-sponsored training education assistance social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds which may include an individuals gender race color national origin ancestry religion creed physical or mental disability marital status sexual orientation medical condition veteran status and age unless such protection is prohibited by federal state municipal provincial local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.

Required Experience : Senior IC

Key Skills: CCTV, Airport Security, Analysis, Higher Education, Jewellery, Jboss

Employment Type : Full-Time

Experience : years

Vacancy : 1