Clinical Study Manager
Artech Information Systems LLC
Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• Provide operational leadership for assigned trials executing them on time and within budget• Overall coordination and management of clinical trials from startup to closeout• Liaise with other functional areas to identify issues, evaluate and make sound business decisions and ensure implementation of timely solutions.• Identify and select high-quality clinical vendors in conjunction with the appropriate team members• Work with the contracting/budgeting team to ensure that vendor responsibilities and payment terms are clearly defined.• Manage and effectively provide oversight of assigned clinical vendors and functional service providers to ensure data integrity and adherence with regulatory requirements.• Assure that team is receiving high quality, on time deliverables from internal and external vendors.• Collaborate with other team members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed consent documents, study management plans and final clinical study reports.• Work with finance manager on financial aspects of the project(s), including milestone payments, and monthly pass through invoices• Lead or facilitate teleconferences with internal or external group.• Oversee Clinical Trial Coordinator for assigned project to ensure successful management of project(s), including development of the project plan, maintenance of trackers, and generation of metrics reports• Assume co-monitoring responsibilities as needed.• Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to proactively recognize problem situations and work with other team members as required to resolve issues• Manage the publication process in conjunction with the publications team to assure that submission timelines are met.• Monitor and report clinical trial status using standard and adhoc review & reporting procedures and identify issues that affect functions. • Ensure that each function is accountable for their deliverables.• In collaboration with Project Management and utilizing various tracking mechanisms, manage clinical trial project milestones and budget. • Proactively identify issues and escalate to appropriate managers.Qualifications• At least 10 years of experience in the management of clinical trials, significant knowledge of overall clinical drug development and general clinical research operations in Big Pharma.• Ability to manage multiple projects simultaneously with strong organizational and planning skills.• Well-developed analytical and problem solving skills. Communicates issues to Director with action plans for resolution.• Knowledgeable in all required regulatory and compliance standards and guidelines including ICH-GCP.• Ability to effectively work with teams and promote collaborations. Exceptional interpersonal skills including the ability to influence negotiate and resolve conflicts.• Excellent verbal and written communication skills and the ability to interact with all levels of management within the organization and to external business contacts. Experience using the Inform database, PowerPoint and Excel software.• Independent judgment and decision making skills with respect to functional responsibilities. Innovative and motivated in optimizing clinical operations processes to meet deliverables.• Minimum BS or BA in related field; focusing on biological science or nursing preferred or equivalent. Advanced Degree preferredAdditional InformationFor more information, Please contact:Sneha Shrivastava973 967 3348SummaryType: ContractFunction: ResearchExperience level: DirectorIndustry: Pharmaceuticals
- ...executing them on time and within budget• Overall coordination and management of clinical trials from startup to closeout• Liaise with other... ...members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed...SuggestedWork at officeImmediate start
$215k - $408.5k
...Director to direct and coordinate the medical management, quality improvement and credentialing... .... Collaborates effectively with clinical teams, network providers, appeals team,... ...policies. Identifies utilization review studies and evaluates adverse trends in...SuggestedFull timePart timeWork at officeRemote workFlexible hoursWeekend work- ...review of listings), SAE reconciliation, managing local laboratory and external labs and... ...Perform Project Management : represent DM on clinical teams, coordinate deliverables by other... ...some experience in supporting Oncology studies. Must be able to work independently....SuggestedLocal areaImmediate start
- ...Clinical Supplies ManagerParamus, New Jersey, United StatesAbout the Job Clinical Supplies... ...and support the Associate Director in managing Contract Development and Research Organizations... ...request forms for new and existing studies when its need it.Prepare requests for...SuggestedContract workWork at office
- ...NS Pharma Inc., Paramus, NJ, is hiring a Manager, Clinical Research to support global clinical studies in a hybrid role. The position requires coordinating study activities, overseeing vendors, and ensuring regulatory compliance. The role emphasizes collaboration with...Suggested
- ...Job Title- Manager, Clinical Science - Contractor Location: Basking Ridge, NJ 07920 Duration: Contract till May 2027 with possibility... ...forms, and clinical sections of submission documents. Performs study level data cleaning of listings and patient profiles. Represents...Contract workFor contractorsRemote work
$150k - $175k
...Director to lead high‑quality veterinary care in a well‑equipped clinic near NYC. You'll join a supportive team with 1 full‑time doctor... ...benefits package and opportunities for teaching and clinical studies, with open seven days a week scheduling. #J-18808-Ljbffr...Full timePart time- ...assistance where applicable. This structure reflects a commitment to clinical excellence, professional growth, and overall physician well-... ...within the organization. As a member of the senior management team, you will work with other members of the team to help develop...Relocation packageMonday to Friday
$150k - $175k
...the care team Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits Benefits | VCA... ...qualifications required of associates assigned to this job. Management reserves the right to revise the job description or require...Full timeFlexible hoursAfternoon shift- ...Senior Trauma Clinical Data CoordinatorOur team members are the heart of what makes us better... ...for the oversight of the data management for the Department of Trauma at Hackensack... ...for all assigned Trauma clinical research studies. This role also supports the Trauma Program...Full timeWork at office
- ...and a commitment to holistic well-being. Role Description The Clinical Program Director is a full-time, on-site role based in Oradell,... ...Day-to-day responsibilities include supervising clinical staff, managing caseload distribution, and monitoring treatment plans to align...Full timeWork at office
$189.2k - $315.4k
...vaccine development program. This role may serve as a clinical lead for one or more studies within a clinical program and works closely with the global... ...of responsible AI practices, including risk management and ethical use.Preferred QualificationsDocumented work...Contract workWork experience placementInternshipH1bVisa sponsorshipWork visaRelocation package2 days per week$150k - $175k
...and the care team Opportunities to participate in a robust Clinical Studies program Benefits: We offer competitive compensation along with... ...qualifications required of associates assigned to this job. Management reserves the right to revise the job description or require...Full timeFlexible hoursAfternoon shift- ...Feel free to check us out at Job Description Title: Clinical Data Manager Location: Woodcliff Lake, NJ Duration: 1 year (... ...management functions to ensure timely and quality database lock for studies Phase I-III. • Perform data management activities for EDC...Contract work
$29.34 - $36.67 per hour
...Summary Coordinates and administers research study associated activities under the direction of... ...Investigator (PI) and Research Nurse Manager/Supervisor. Assists in project planning; coordinates and implements clinical research; acts as the patient advocate by assuring...Hourly payFull timeTemporary workPart timeLocal areaFlexible hoursShift work- ...Clinical Pharmacology Associate DirectorThe Clinical Pharmacology (CP) Associate Director... ...pharmacokinetic/pharmacodynamic (PK/PD) studies. This individual will participate in the... ...early and late-stage clinical and lifecycle management projects/programsProvide support in the...
- ...Job Description Job Description We are seeking a dedicated and experienced Clinical Manager (RN) to oversee the quality of care for our pediatric home health clients. This is an in-office position responsible for case managing our pediatric clients who are served...Work at officeRelocation package
- Summit Clinical Research Solutions in Ridgewood, NJ seeks a Clinical Research Coordinator to manage trial operations, recruit/screen participants, and ensure protocol and regulatory... ...and data integrity across multiple studies. The role reports to the Clinical Operations...
- The Senior Trauma Clinical Data Coordinator is responsible for the oversight of the data management for the Department of Trauma at Hackensack University Medical Center (HUMC... ...for all assigned Trauma clinical research studies. This role also supports the Trauma Program under...Full timeWork at office
$150k - $175k
...Veterinary Medical Director to lead its clinical team while continuing to practice high-quality... ...Senior pet care Chronic disease management Urgent medical cases The caseload... ...Participation in clinical research and studies Career advancement pathways Qualifications...Full timePart timeLocal areaMonday to FridayFlexible hoursAfternoon shift- ...firm serving clients throughout the United States. KCI is recognized as an industry leader, employing cutting-edge technologies, management practices and strategic growth initiatives. Employee ownership fosters an entrepreneurial spirit, encourages technical expertise,...Contract workFor contractorsWork experience placementLocal area
$88.6k - $132.89k
...the way. Find a home for your career here. Join us and embrace a culture of Caring. Connecting. Growing together. As the Clinical Manager, you will provide leadership, supervision, and coordination of therapy services to ensure high-quality, compliant, and cost-...Minimum wageFull timeWork experience placementLocal areaImmediate startRelocation package$108.78k - $135.99k
...POSITION SUMMARY Responsible for managing the Inpatient/Outpatient Coding staff. Responsible for all coding related functions. Must be subject matter expert in all software used. Responsible for timely completion of accurate and complete coding to support Valley Hospital...Full timeTemporary workPart timeLocal areaFlexible hoursShift work$172k - $275.2k
..., and staff, as directed by the VP, EP Hires, evaluates and manages EP associates, contractors and/or vendor personnel who engage in... ...expertise to the project team and effectively manage assigned clinical site(s)/project(s) Oversee and ensure site staff execute protocols...Daily paidTemporary workFor contractorsFlexible hours- ...Bergen New Bridge Medical Center in Paramus, NJ seeks a Clinical Manager to lead substance abuse counseling services, ensure evidence-based practices, and supervise clinical staff. The role focuses on developing policies, coordinating care, and maintaining quality standards...Full timeFlexible hours
$84.04k - $151.36k
...laboratory personnel in meeting the standards for clinical testing Ability to lead subordinate staff... ..., staff and customers. Ability to manage multiple engagements concurrently. Strong... ..., e. g., surveys, statistical reports, studies, research, etc. About the organizationQuest...Full timeTemporary workPart timeWork experience placementMonday to FridayFlexible hoursShift workWeekend work$175k - $205k
...cutting-edge science as a subsidiary of Nippon Shinyaku Co., Ltd. In Japan. Summary Responsible for the management and execution of various aspects of clinical studies (implementation, site selection, patient recruitment, vendor oversight, tracking clinical data, etc.)...Temporary workFlexible hours$210.4k - $331.1k
...and/or investigator-sponsored research studies. The Regional Medical Scientific Director... ...comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest... ...and dialogue Excellent stakeholder management, communication, and networking skills A...For contractorsWork at officeLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work- ...firm serving clients throughout the United States. KCI is recognized as an industry leader, employing cutting‑edge technologies, management practices and strategic growth initiatives. Employee ownership fosters an entrepreneurial spirit, encourages technical expertise,...Contract workWork experience placementLocal area
- ...firm serving clients throughout the United States. KCI is recognized as an industry leader, employing cutting-edge technologies, management practices and strategic growth initiatives. Employee ownership fosters an entrepreneurial spirit, encourages technical expertise,...Contract workWork experience placementFlexible hours
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