What are the responsibilities and job description for the Clinical Study Administrator, Country Operations Management position at Syneos Health?
Description
Clinical Study Administrator, Country Operations Management
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
Clinical Study Administrator
Location: Boston, MA (Seaport area)
Role Summary:
We are seeking a skilled and motivated CSA to join our sponsor-dedicated team supporting rare disease trials. In this role, you will work full-time on behalf of a leading sponsor while employed within a global CRO - offering the best of both worlds: sponsor collaboration and CRO resources.
What You Will Do:
The CSA collaborates closely with the Project Manager Country Operations and other local study team members such as the Study Start Up manager, Clinical Research Associates, Site Management Leads and Head of Country Operations in delivering support in the conduct of clinical trials in region or country.
You will be responsible for:
Salary Range:
The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
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.
Summary
We are seeking a skilled and motivated CSA to join our sponsor-dedicated team supporting rare disease trials. In this role, you will work full-time on behalf of a leading sponsor while employed within a global CRO - offering the best of both worlds: sponsor collaboration and CRO resources.
Clinical Study Administrator, Country Operations Management
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.
Clinical Study Administrator
Location: Boston, MA (Seaport area)
Role Summary:
We are seeking a skilled and motivated CSA to join our sponsor-dedicated team supporting rare disease trials. In this role, you will work full-time on behalf of a leading sponsor while employed within a global CRO - offering the best of both worlds: sponsor collaboration and CRO resources.
What You Will Do:
The CSA collaborates closely with the Project Manager Country Operations and other local study team members such as the Study Start Up manager, Clinical Research Associates, Site Management Leads and Head of Country Operations in delivering support in the conduct of clinical trials in region or country.
You will be responsible for:
- Providing support to the local study team in COM in achieving quality and timeliness of study deliverables across the lifecycle of assigned trials (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation)
- End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the Clinical Trial Management System (CTMS) and other general trial support in the country or region as delegated or per assigned trials.
- Providing support to the local study team including for start up activities in start-up phase: CDA delivery and negotiation, distribution and collection of documents, communication with sites during contract negotiation phase, Site File preparation and preparation and approval of sites for activation, etc
- Collaborating with PMCO, CRAs, SSU manager and study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information
- Act as a central point of contact for the local study team in COM for designated project communications, correspondence, and associated documentation.
- Input on the development and maintenance of project management and other global tracking tools (e.g: CTMS, smartsheets, etc).
- Collaborating in global initiatives to standardize processes within and across countries (collaboration with other local and global CSAs)
- Assist with local language translations, IRB/CEC/CA submissions in collaboration with Regulatory Affairs and other functions, as required within the country/region.
- Providing support to local COM team with local F2F study and team meetings (venue, cost, agenda, etc), support team teleconferences, assist with staff onboarding as required by country/region
- Bachelor's Degree in a related discipline, preferably life science.
- Proficiency with MS Office Suite (excel, word, powerpoint)
- Understanding of the drug development process either via education or experience in the life sciences field.
- 1 years of experience in the pharmaceutical industry working with delivery of clinical studies.
- Excellent collaboration and interpersonal skills, unafraid to ask questions.
- Strong organizational skills and ability to manage competing priorities.
- Strong attention to detail
- Effective written and verbal communication skills
Salary Range:
The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
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.
Summary
We are seeking a skilled and motivated CSA to join our sponsor-dedicated team supporting rare disease trials. In this role, you will work full-time on behalf of a leading sponsor while employed within a global CRO - offering the best of both worlds: sponsor collaboration and CRO resources.