Research operations occupations Work, Jobs in Teddington, Gtl (with Salaries)

Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge.
Syneos - Clinical and Corporate - Prod —London
- Full-time
- PMP
- Project management
- Bachelor's degree
Data Coordinator (London, Entry-Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
Research Administrator
Great Ormond Street Hospital for Children —London
- £34,186 - £37,389 a year
- Part-time
- Computer literacy
- Administrative experience
- Organisational skills
8d
Research Assistant
University College London —London
- £39,148 - £41,833 a year
- Full-time
- Bachelor's degree
- Quality control
- Organisational skills
- Annual leave
- Employee assistance programme
9d
eClinical Coordinator (London)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
Trial Coordinator
ICR —London
- £31,445 - £33,600 a year
- Travel
- IT
10d
Research Assistant (Neuroimaging)
University College London —London
- £39,148 - £41,833 a year
- Full-time
- Bachelor's degree
- Communication skills
- Annual leave
- Employee assistance programme
1h
Senior Impact Officer
University of Surrey —Guildford
- £37,694 - £42,254 a year
- Full-time
- Hybrid work
- University
- Organisational skills
- Communication skills
- Relocation assistance
- Annual leave
1d
Research Facilitator
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Free parking
6d
Clinical Research Coordinator
Velocity Clinical Research, Inc. —High Wycombe
- £30,000 - £40,000 a year
- Full-time
- Nursing
- Microsoft Office
- Bachelor's degree
- Free parking
- Health & wellbeing programme
Quick apply
5d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Program Officer, AI for Health
PATH —London
- Full-time
- Bachelor's degree
- Travel
- Communication skills
6d
Head of Virology (ID4520)
Animal and Plant Health Agency —New Haw
- £73,165 - £81,535 a year
- Overtime
- Doctoral degree
- Presentation skills
- Leadership
- Annual leave
- Employee discount
9d
Research Communications Co-Ordinator
University College London —London
- £36,433 - £41,833 a year
- Full-time
- Administrative experience
- Communication skills
- Annual leave
- Employee assistance programme
13h
Clinical Trial Manager at CCTU
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Travel
- Communication skills
- Time management
- Annual leave
- Employee assistance programme
13d
Clinical Assistant (Trials)
ICR —London
- £31,445 - £33,600 a year
- Call to connect
- Customer service
- Microsoft Office
- Organisational skills
1d
Centre Manager
SOAS University of London —London
- £43,297.57 - £50,562.57 a year
- Full-time
- Master's degree
- School
- Annual leave
- Employee assistance programme
7d
Research Support Administrator
Buckinghamshire New University —High Wycombe
- £26,093 - £28,778 a year
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Administrative experience
- Employee discount
2d
Data Curator
ICR —Sutton
- £31,445 - £33,600 a year
- Hybrid work
- SQL
- Linux
- Communication skills
2d

I want to receive the latest job alerts for research operations occupations in teddington, gtl

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge.

Syneos - Clinical and Corporate - Prod -
London

Apply Now

Job details

Full-time

Qualifications

PMP
Project management
Bachelor's degree
Organisational skills
Contracts
Communication skills

Full job description

Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge.

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Plan, direct, create, and communicate clinical study timelines to ensure deliverables are produced on schedule. This includes developing detailed project plans, setting milestones, and coordinating with cross-functional teams to ensure timely completion of tasks
Gather input from cross-functional teams to create comprehensive plans for clinical studies. This involves collaborating with departments such as regulatory affairs, data management, and clinical operations to integrate their feedback into the study plans
Ensure consistency of clinical study processes across clinical trials, adhering to standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations. This includes developing and implementing standardized processes and procedures to ensure uniformity across all trials
Oversee and resolve operational aspects of clinical trials in conjunction with project teams. This includes identifying and addressing any issues that arise during the trial, coordinating with team members to implement solutions, and ensuring that the trial stays on track
Select sites and vendors, prepare clinical trial budgets, and ensure studies are conducted within clinical trial protocols. This involves evaluating potential sites and vendors, negotiating contracts, and managing budgets to ensure that the trial is conducted within the allocated resources
Monitor progress and follow up with team members and line managers when issues develop. This includes tracking the progress of the trial, identifying any deviations from the plan, and working with team members to address any issues that arise
Implement and prepare the clinical development strategy as outlined by the clinical teams. This involves developing and executing strategies to achieve the clinical development goals, coordinating with clinical teams to ensure alignment, and monitoring progress towards these goals
Develop trial recruitment strategies to ensure successful participant enrollment. This includes identifying target populations, developing recruitment plans, and implementing strategies to attract and retain participants

Qualifications:

Bachelor's degree in a related field (e.g., Clinical Research, Life Sciences, Healthcare Management)
Minimum of 5 years of experience in clinical project management or a related role
Proven track record of successfully managing clinical trials and ensuring adherence to SOP, GCP, and country regulations

Certifications:

Certification in Clinical Research (e.g., CCRP, CCRA) is preferred
Project Management Professional (PMP) certification is a plus

Necessary Skills:

Strong organizational and planning skills to create and manage clinical study timelines
Excellent communication skills to gather input from cross-functional teams and communicate plans effectively
Ability to oversee and resolve operational aspects of clinical trials
Knowledge of SOP, GCP, and country regulations to ensure consistency across clinical studies
Experience in site and vendor selection, budget preparation, and monitoring progress
Ability to implement and prepare clinical development strategies
Strong problem-solving skills to address issues that arise during clinical trials

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Apply Now

Refine Your Search

research operations occupations jobs in teddington, gtl

Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge.

Data Coordinator (London, Entry-Level)

eClinical Coordinator (London, Entry Level)

Research Administrator

Research Assistant

eClinical Coordinator (London)

Trial Coordinator

Research Assistant (Neuroimaging)

Senior Impact Officer

Research Facilitator

Clinical Research Coordinator

Specialist, R&D Contracts & Business Operations

Program Officer, AI for Health

Head of Virology (ID4520)

Research Communications Co-Ordinator

Clinical Trial Manager at CCTU

Clinical Assistant (Trials)

Centre Manager

Research Support Administrator

Data Curator

I want to receive the latest job alerts for research operations occupations in teddington, gtl

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected