Clinical Study Project Manager
SGS
Company DescriptionSGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.Job DescriptionThe Study Project Manager is ultimately accountable for the planning, execution, issue resolution, and communication / communication planning required for successful execution of each assigned clinical study or designated internal project.This includes holding planning meetings as needed with test facility or other personnel regarding study/project design, contract, timeline for prestudy activities (such as schedule, protocol, ethics committee, recruiting, documents, and data management), study/project execution, data analysis and clinical study report/other deliverables, and archiving. During study/project execution, the Study Project Manager tracks project activities against the schedule, orchestrates all functions to identify and remove roadblocks, anticipates and resolves issues, and coordinates the participation of external resources. The Study Project Manager may conduct a post-mortem analysis. The Study Project Manager is the central point of communication to the study Sponsor or project requestor, and sends updates on a scheduled basis including information from all relevant functional areasEstablish a standard project dashboard to show standard phases each study may go through in addition to visual status, timeline, and risk information. This may include a version that can be shared with clients as a standard scheduled update. Establish a detailed project plan for each assigned study to coordinate and track execution with the appropriate functional teams. Run a weekly Project Management / Study Scheduling meeting to provide status updates, gather input for scheduling of new studies, escalate issues, and align on client communications / communication plans as needed Facilitate discussions for issue resolution by pulling together the needed experts and driving to consensus on the path forward, when required Communicate status or updates to project sponsors, or coordinate updates with the relevant Global Key Account Manager (GKAM) Suggest improvements to our study execution process based on observed inefficiencies or identified opportunities Complete training within required deadline Adhere to internal standards, policies, and proceduresQualificationsBachelor’s degree (science, business, or project management preferred)6-18 months clinical research experience or equivalent2+ years of project management experienceAbility to learn and use MS Project or other project management platform Strong understanding of clinic processes and flow, and ability to create study schedules that make good use of resources Ability to work with others to communicate requirements, build consensus, and overcome problems Excellent ability to establish priorities with minimal supervision and attention to detail Additional InformationSGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call View phone number on click.appcast.io for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.SummaryType: Full-timeFunction: ScienceExperience level: Mid-Senior LevelIndustry: Pharmaceuticals
- NOTE: No C2C Candidates can be considered for this role. Must have Cerner Implementation experience. Title: Clinical Project Manager - Remote (10-20% Travel) Type: Contract - Full-Time Duration: 12 Months (with potential for extension) Location: Remote (10-20% travel...SuggestedFull timeContract workRemote work
$120k - $135k
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- ...facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical Practices (GCP),... ...for all other studies Assures that staff working on their managed studies understand and are performing duties according to...SuggestedWork experience placement
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- ...Position Summary: The Research Coordinator is responsible for managing multiple clinical research protocols while serving as a key liaison between... ...: Coordinate daily operations of research studies from feasibility through closeout. Act as liaison between...Local areaShift work
- SGS in Richardson, TX is seeking a Clinical Study Coordinator to coordinate and facilitate daily activities in clinical studies in accordance... ...set up studies, prepare and organize study documentation, manage subject scheduling, assist IRB submissions, mentor new clinic...
- ## SR Clinical Project ManagerUS, Remote · Full-time#### About The PositionInsightec is a growing medical technology company transforming... ...Responsible for independently leading the clinical trial study team and managing global clinical trial activities on a pivotal trial or...Full timeContract workTemporary workLocal areaRemote workFlexible hours
- SGS is seeking a dedicated professional to coordinate and facilitate clinical studies in Richardson, Texas. The position involves ensuring compliance with clinical protocols and regulations, maintaining detailed documentation, and training new staff. The ideal candidate...
- SGS is looking for a Clinical Research Coordinator located in Richardson, Texas, to... ...lead coordination on various clinical studies. The role involves performing... ...solving abilities. This position requires managing multiple projects in a fast-paced environment. #J-1880...
$23 - $30 per hour
...Job Description Title: Clinical Research Coordinator I, II or... ...the coordination of clinical studies and execute ongoing follow-up... ...SOPs, and GCP guidelines. Manage daily operational tasks such... ...issues with panelists, arrange project work, and assist with additional...Full timeTemporary workLocal area- SGS in Richardson, TX seeks a hands-on Clinical Research Assistant to manage test materials, coordinate staff schedules, and archive study documents. The role requires collaboration... ...experience; ability to manage multiple projects in a fast-paced environment; and basic understanding...
- Job Title & Specialty Area: Clinical Research CoordinatorDepartment... ...trials, as well as observational studies conducted at Children's... ...serves as the Children's employee managing the coordination of all aspects of the assigned research project(s) at Children's in support...Full timeWork experience placementLocal areaRemote workMonday to FridayShift work
- ...supervision, to coordinate research projects. This position primarily... ..., however, may conduct data management in smaller departments on as... ...and ensures quality control of clinical or basic research data in... ...multiple and/or complex research studies. The position will be for a...Full timeLocal area
- ...supervision, to coordinate research projects. This position primarily... ..., however, may conduct data management in smaller departments on as... ...and ensures quality control of clinical or basic research data in... ...multiple and/or complex research studies. BENEFITSUT Southwestern is...Full timeContract work
- ...supervision, to coordinate research projects. This position primarily... ..., however, may conduct data management in smaller departments on as... ...and ensures quality control of clinical or basic research data in... ...multiple and/or complex research studies. The Clinical Research...Full timeLocal area
- Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking... ...Submissions Coordinator to join our Study Start-up team. This position works both... ...plays a key role in the clinical trial management and study start-up process at Medpace. We...Full timeContract workWork at officeLocal areaImmediate start
- Lead Clinical Research Coordinator- Psychiatry Department - Molecular Imaging DivisionWHY... ...the operational backbone for PET and MRI studies designed to clarify the biology of... ...stewardship of tightly coordinated visits, managing imaging and clinical data, ensuring regulatory...Full timeLocal area
$22.5 - $25 per hour
...Clinical Research Coordinator PM Pediatrics Urgent Care, Dallas... ...Resistance is a clinical trial site management organization that performs... ...of clinical research projects, ensuring the successful attainment... ...binders, inventory of study-specific and clinical supplies...Hourly payFull timeMonday to Friday- ...Summary : Clinical Research Coordinator 2 is a Part Time or Full... ...procedures for one or more research studies. The CRC2 may supervise less-... ...the research goals of each project. A Coordinator 2 will... ...Coordinates collection and data management of national research studies...Full timePart timeWork at officeLocal area
- ...premier investigational sites meeting the clinical research needs of global... ...organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake... ...with regulatory compliance. Conducting studies since 1984, M3 Wake Research owns a proprietary...Flexible hours
- ...Clinical Research Coordinator II - Relocation to Amarillo, TX Our clinical research company is looking to hire a qualified candidate... ...entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence An...Full timeTemporary workRelocationWork visaFlexible hours
- ...Clinical Research Coordinator (Onsite) Ready to make an impact in medical research? This Clinical Research Coordinator role offers... ...hospital-based clinical trials. The position involves coordinating study activities, collecting data, ensuring compliance, and...Weekday work
$23 - $28.37 per hour
...Clinical Research Coordinator II Join us in shaping the future of clinical research.... ...supporting both inpatient and outpatient studies. We are seeking experienced applicants... ...ideal for coordinators with experience managing one or more trials, supporting day-to-day...Hourly payFlexible hours- ...Clinical Research Coordinator The Clinical Research Coordinator leads and manages clinical trials in compliance with regulatory standards, working closely with the investigative... ...patient visits and ensure adherence to study protocols, collecting and processing...Work at office
- SGS in Richardson, Texas is seeking a Clinical Research Coordinator I (CRC I) to lead studies and perform essential tasks. Responsibilities include coordinating... ...experience, with skills in research and project management. This role requires multitasking and adherence to...
- ...Visa : USC, GC Position Overview The Senior Clinical Trial Manager provides strategic and operational leadership for global clinical... ...trials. This role leads Clinical Trial Managers and study teams to ensure successful planning, execution, and delivery...
- ...for a full-time, office-basedAssociate Clinical Trial Manager (aCTM) to join our Clinical Trial... ...Clinical Trial Management team and support Project Coordinators and Clinical Trial... ...ResponsibilitiesCommunicate and collaborate on global study activities; working closely with the...Full timeContract workWork at officeLocal areaImmediate start
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