Study Activation Specialist

McKesson; United States; On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits

Annual bonus potential

Equity / long-term incentive

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Study Activation Specialist to oversee startup activities for clinical trials across multiple sites in the U.S. You will build relationships with sponsors, CROs, and internal teams to ensure timely study activation and protocol adherence.

The role requires knowledge of pharma, regulatory processes, and clinical trials, plus at least 1 year in client-facing customer service.

Qualifications

• High School Diploma required; Bachelor Degree preferred.
• Knowledge of pharmaceutical industry, regulatory processes, clinical trials and medical terminology.
• The availability to travel occasionally.
• At least one year of experience in Customer Service in a Client Facing Role.
• Experience in healthcare, research, pharmaceutical or marketing industries preferred.

Responsibilities

• Manage the startup activities of clinical trials proposed and entering those trials into SCRI's program menus.
• Maintain relationships and facilitate progress across multiple groups including internal SC departments, Strategic Sites physicians and staff, CROs, and Pharmaceutical Companies.
• Serve as the primary responsible party and point of contact during feasibility, planning, and implementation stages up to site activation.
• Develop relationships with sponsors and CROs to provide potential studies.
• Market SCRI services and capabilities to pharmaceutical companies, CROs and the industry network.
• Track site metrics related to the study startup process for each Strategic Site.
• Other duties as assigned.

Skills

Customer service

Healthcare knowledge

Regulatory knowledge

Clinical trials

Travel flexibility

Education

Bachelor's degree

Job description

It's More Than a Career, It's a Mission.

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.

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.

Total Rewards

We care about the well-being of the patients and communities we serve, and that starts with caring for our people.

• includes comprehensive benefits to support physical, mental, and financial well-being.


• competitive compensation package.


• 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.

Key Responsibilities

• As the Study Activation Specialist, you are responsible for managing the startup activities of clinical trials proposed and entering those trials into the Sarah Cannon Strategic Sites' clinical research program menus.


• You will maintain relationships and facilitate progress across multiple groups including but not limited to internal SC departments, Strategic Sites physicians and staff, Contract Research Organizations (CROs), and Pharmaceutical Companies.


• You will serve as the primary responsible party and point of contact during clinical research trial feasibility, planning, and implementation stages up until the point of site activation.


• You will develop relationships with sponsors and (CROs), which provide potential studies


• You will maintain a database of potential pharmaceutical and CRO relationships


• You will market Sarah Cannon services and capabilities to pharmaceutical companies, CROs and within the industry network


• You will develop and maintain strong industry ties, utilizing both the network and the Internet, in order to acquire new studies


• You will provide information and updates on current studies in the start-up process at all Sponsor meetings


• You will track all site metrics relating to the study start up process for each Strategic Site


• Other duties as assigned

Qualifications

• High School Diploma required; Bachelor Degree preferred


• Knowledge of pharmaceutical industry, regulatory processes, clinical trials and medical terminology


• The availability to travel occasionally


• At least one year of experience in Customer Service in a Client Facing Role
  
• Experience in healthcare, research, pharmaceutical or marketing industries preferred

20+ states across the U.S.