Manager or Research Study Activation
McKesson’s Corporate
Manager of Study Activation As Manager of Study Activation at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will oversee all study activation activities, supervise the activation team, and ensure compliance with standard operating procedures, FDA guidelines, and GCP. Responsibilities Overall study activation activities, including direct supervision and development of staff, adherence to SOPs, and reporting data to internal and external stakeholders. Lead study start‑up activities, covering trials in lead, opportunity, and selection. Oversee the study activation team and coordinate with site, sponsor and CRO contacts to establish and maintain key connectivity. Support the site evaluation process from opportunity review through executive leadership recommendation. Interface with Sarah Cannon lines of business to develop relationships and understand business line needs, providing high‑level service and site collaboration. Facilitate business development and relationship‑management activities with pending and active sites and pharma/CRO partners. Utilize metrics to drive improvement strategies for trial activations and stakeholder relationships. Escalate unresolved issues to Senior Manager or appropriate level of management. Drive new initiatives and special projects as directed by Senior Manager, Site Relationships and Support Services. Provide oversight, leadership and direction for study start‑up of trials and maintenance areas where support is provided. Assess organizational processes associated with start‑up and support to identify improvements and streamline processes. Meet with site leadership as needed to ensure contracted services are being delivered. Qualifications Ability to read, understand and comply with research protocols. Knowledge of FDA guidelines and Good Clinical Practice (GCP). Resourceful with strong analytical and problem‑solving skills in a fast‑paced environment. Excellent interpersonal skills, detail‑oriented and meticulous. Clinical and/or scientific experience in a research setting (required). Research certification (ACRP or CCRP) preferred. Equal Opportunity Employer We are an equal‑opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. #J-18808-Ljbffr McKesson’s Corporate
- ...our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have... ...research, SCRI is redefining cancer care around the world. Manager of Study Activation As the Manager of Study Activation you will be responsible...Suggested
- ...Job Summary: The Clinical Laboratory Study Manager works with Precision Medicine Strategy... ...teams and sub-teams across clinical and research departments Works with clinical... ...and testing Participates in oversight activities with vendors and other collaborators, and...SuggestedRemote work
- ...serves as Health Science Specialist - Research Study Coordinator within the Research and Development... ...with knowledge of the full scope of activities required in conducting single and/or... ...research including study/project management, human subjects' protection, and regulatory...SuggestedFull timePart timeWork at office
- ...serves as Health Science Specialist - Research Study Coordinator within the Research and Development... ...with knowledge of the full scope of activities required in conducting single and/or... ...research including study/project management, human subjects' protection, and regulatory...SuggestedPermanent employmentFull timeTemporary workPart timeWork at officeRelocationRelocation packageMonday to Friday
- ...of Veterans Affairs is seeking a Health Science Specialist - Research Study Coordinator to support clinical research within its Research... ...Responsibilities include participant recruitment, protocol execution, data management, and ensuring regulatory compliance. #J-18808-Ljbffr US-...Suggested
- Direct Jobs is seeking a Clinical/Translational Research Coordinator II (CTRC II) in Nashville, TN. In this role, you... ...relevant research experience. Responsibilities include managing IRB applications, conducting study procedures, and ensuring regulatory compliance. This...Monday to Friday
$92k - $105k
Position Overview: Now Hiring: Research Director Location:... ...stakeholder engagement, data management, and dissemination of findings... ...collection, management, and analysis activities Maintain high scientific,... ...initiatives and multi-site studies ~ Experience managing...Full timeTemporary workImmediate start- ...Research Nurse Manager Tennessee Oncology, one of the nation's largest, community-based cancer... ...supervising, evaluating, and coordinating the activities of a team of professional nurses and/... ..., from protocol review/initiation to study close-out, ensuring study integrity...Work at officeLocal area
- ...Supports and coordinates clinical research studies within the Radiology department. Ensures protocol compliance, manages study activities, and serves as a key liaison between internal teams, investigators, and external partners. Key Responsibilities: Coordinate and manage...
- Research Nurse Manager The Research Nurse Manager ensures the integrity and quality of clinical trials... ..., evaluating, and coordinating the activities of a team of professional nurses and/or... ..., from protocol review/initiation to study close-out, ensuring study integrity throughout...Work at officeLocal area
$195.5k - $244.4k
...aim to accelerate discovery, research, and development to bring novel... ...of one or more clinical studies within a program(s), ensuring... ...reporting. Proactively identify, manage, and mitigate study/program... ...lead quality and compliance activities with cross-functional teams...For contractorsWork at officeRemote workWorldwideFlexible hours- ...an exciting opportunity for a Sr. CTM. This candidate is responsible for : Manages all operational aspects for implementation of one or more clinical trials and all activities from study start-up through database lock, ensuring Good Clinical Practices (GCP) and relevant...Contract workRemote work
- ...Senior Clinical Project Manager – Oncology/Hematology (Phase III)... ...advancing oncology and hematology research? Do you thrive in a fast‑... ...accountability across all vendors and study partners. Implement... ...professional development are actively encouraged. If you are...Contract workRemote work
$192.32k - $240.4k
...aim to accelerate discovery, research, and development to bring novel... ...executing clinical research activities in various indications... ...clinical development planning; manage CDP, LRP, internal governance... ...education of investigators, study site personnel, and study staff...Work at officeRemote workWorldwideFlexible hours$284.32k - $355.4k
...- to late-stage assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner... ...and Responsibilities ~ Responsible for and lead all activities related to clinical study design from clinical study concept to clinical study...WorldwideFlexible hours$310k - $375k
...Medical Director - Clinical Research About Pharming Pharming... ...global clinical research and activities for napazimone and other Pharming... ...strategy, develop protocols, study start-up, close-out,... ...clinical development including managing CROs ~ Experience in product...Temporary workWork experience placementRemote workFlexible hours- ...Description POSITION TITLE: Clinical Research Coordinator I DEPARTMENT:... ...during clinical research study visits while ensuring... ...Coordinators and Clinical Project Managers to execute protocol... ...Participate in study start-up activities such as putting together charts...Daily paidFull timeContract workFlexible hours
- Job Description The Research Coordinator I will assist in the management of subjects on clinical trials and coordinate activities associated with clinical trials under the mentorship of... ...of each patient for the duration of a study Procures, processes, and ships biospecimens...Work at office
- ...patient care, education, and research. Organization: General Pediatrics... ..., ensuring high-quality study conduct, regulatory compliance... ...study operations; coordinate activities across multiple clinical sites... ..., when due, from project managers for all approved projects. Provides...Temporary workFor contractorsTraineeshipWork experience placementWork at officeRemote workMonday to Friday
- Equity Medical is growing, and we are actively seeking an experienced Clinical Research Coordinator to join our new Nashville, Tennessee site. Equity... ...ideal candidate will have experience independently managing studies, working directly with sponsors and CROs, and...
- ...Nashville, TN, we are seeking a Clinical/Translational Research Coordinator II to manage interventional and observational studies. This role involves preparing IRB applications, conducting participant engagement activities, and ensuring compliance with Good Clinical...Casual workMonday to Friday
- Overview Clinical Project Manager II - Virology (Sponsor Dedicated - US Remote; Preference... ...in the operational details that keep studies running successfully day to day? This is... ...operationally. You should be comfortable actively reviewing study documentation, managing...Remote jobContract workWork from home2 days per week3 days per week
- ...the acceleration of clinical research to transform patient outcomes... ...we empower research teams and study sponsors to expand and... ...coordinates the daily clinical trial activities and plays a critical role in... ...and clinically manage industry‑sponsored clinical trials...Full timeWork at office
- ...and the expertise of clinical research for all patients, at... ...regulatory compliance, optimizes study execution, and drives growth... ...Implement, optimize, and manage department-specific technology... ...Assistant Directors to manage daily activities while maintaining strategic oversight...
- ...oncologists and the patients they serve. Job Description: The Manager, Research Quality will report to the Sr. Manager, Research Quality .... ...for leading quality assurance and research compliance activities at the site level by serving as the primary expert on current...Work at office
$4,144.04 - $4,583.33 per month
.../ Essential Job Functions The Research Project Coordinator plans, directs, and coordinates activities to ensure the successful administration... ...resource collection, storage, management, auditing, and security as... ...records of implementation of study activities according to...Weekend workAfternoon shift- ...patient care, education, and research.Organization:Allergy, Pulmonary... ...and motivated Lab Manager to join our dynamic clinical-... ...opportunity to work on groundbreaking studies, collaborate with leading experts... ...Impact: Directs activities to achieve operational plans...Temporary workWork experience placement
- ...cancer care and the expertise of clinical research for all patients, at convenient locations... .... Key Responsibilities and Duties Manage, date and distribute all incoming departmental... ...paper if required and electronic for all new studies. Prepare initial regulatory packet to...Interim roleLocal area
$85k - $90k
Research Coordinator: Engineering Research, Tickle College of Engineering - UTK Knoxville, TN, United States (Hybrid) Job Description... ...enterprise. Responsibilities The Research Coordinator will have an active role in implementing efforts to enhance the success of faculty...Full timeContract workWork at officeWork visa$27.65 - $43.55 per hour
Job Description The Clinical Research Project Coordinator supports the Research Billing... ...Analyses (MCAs), overseeing billing activities for research studies, ensuring accurate and timely... ...member when needed. Budget & Scope Management: Develop comprehensive budget and scope...Hourly payWork at officeFlexible hoursNight shift
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