Manager or Research Study Activation
McKesson
It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world. Manager of Study Activation As the Manager of Study Activation you will be responsible for overall study activation activities, including direct supervision and development of staff, adherence to standard operating procedures and reporting of data to internal and external groups. You will provide leadership in the study start-up, to include trials in lead, opportunity and selection. You will oversee the study activation team You will liaise with site, sponsor and CRO contacts to establish and maintain key organizational connectivity through study start-up You will support the overall site evaluation process from review of opportunity to executive leadership recommendation You will interface with Sarah Cannon lines of business to develop/foster relationships and understanding of business line needs in order to provide high level service and appropriate site collaboration You will facilitate business development and relationship management activities with pending and active sites and pharma/CRO partners You will utilize metrics to drive improvement strategies trial activations for sites and site, sponsor and CRO partner relationships You will appropriately escalated unresolved issues to Senior Manager or appropriate level of management You will drive new initiatives and special projects, as directed by Senior Manager, Site Relationships and Support Services You will provide oversight, leadership, and direction in the study startup of trials and in maintenance areas where support is provided You will assess organizational processes associated with startup and support to identify ways to improve and streamline processes You will meet with site leadership as needed to ensure contracted services are being provided by the teams You should have for this position: The ability to read, understand, and comply with research protocols. Knowledge of FDA guidelines and GCP. Resourceful with heightened analytical abilities and problem solving skills in a fast paced environment. Excellent interpersonal skills, detailed-oriented and meticulous. Clinical and/or scientific experience in a research setting required. Research certification (ACRP or CCRP) preferred. About Sarah Cannon Research Institute Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings. We care about the well‑being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well‑being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here. As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long‑term incentive opportunities may be offered. McKesson has become aware of online recruiting‑related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind: McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application. McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting‑related communications with candidates. McKesson job postings are posted on our career site: careers.mckesson.com. 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
- ...our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have... ...SCRI is redefining cancer care around the world. As the Manager of Study Activation you will be responsible for overall study activation activities...Suggested
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- ...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
- ...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
- ...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
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$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
- 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
- ...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
- ...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
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$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$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$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$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- ...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
- 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
- ...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
- 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
- ...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
$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- ...The Research Data Coordinator is responsible for collecting, transcribing, and transmitting... ...data for multiple investigational drug studies performed. This role provides accurate... ...letters from monitoring visits. Meet data management deadlines as set by both internal and...Contract workWork at office
$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- ...least 1-2 years of experience in a Clinical Research Department setting to join our robust... ...Coordinator A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials... ...delivery. Perform urinalysis during study visits to detect hematuria, infections,...Full timeTemporary workWork at officeLocal areaImmediate startWeekday work
- MD Ally is seeking a full-time Clinical Research Coordinator I to manage daily clinical trial activities. The successful candidate will support industry-sponsored... ...Clinical Practices and enhancing patient safety during studies. MD Ally values inclusivity and diversity in the...Full time
- ...content, purity, stability, and other characteristics of the samples analyzed. The candidate may also perform method development activities related to the development of methods for testing raw materials and clinical drug products as well as formulation development. Responsibilities...Contract workLocal areaFlexible hoursNight shiftAfternoon shift
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