• Collaborating with a group of independent direct store delivery distributors to advance good2grow sales within the assigned territory • Participates in distributor training, sales meeting presentations, ride alongs, etc. • Provides clear follow up notes after ride alongs and store visits • Uses VIP Karma app to track, audit, follow up, and execute store visits • Communicates with key influencers within the distributor organization on major opportunities at the retail level • Develops larger chains, local chains, and the independent market • Penetrates new accounts using targeted void reports as provided by manager or Distributor • Increases good2grow store presence through kids eye level shelving and multiple points of interruption throughout the store • Grows the number of good2grow SKUs available in the market • Completes all administrative duties required on Friday office days in a timely manner

• Provide virtual high-volume omnichannel support through email, chat, text, virtual connections, and inbound or outbound calls to patients, HCPs, REMS vendor, HUB, specialty pharmacy, and field teams • Demonstrate strong empathy and high emotional intelligence to engage patients/HCPs effectively, creating individual relationships built on trust and rapport • Provide proactive support to HCP office issues related to REMS, reimbursement, insurance coverage, and product dispense • Act as a primary point of contact for patients to provide comprehensive disease/therapy education and access to therapy (including benefit verification, prior authorizations, and navigating insurance reimbursement processes) • Prepare structured case status reports for ongoing HCP email or telephonic review • Collaborate and work cohesively with Momentum Inbound team to identify gaps, barriers, and opportunities to improve process and overall patient/HCP experience • Communicate complex information effectively and empathetically to patients/HCPs • Accurately complete patient engagements based on provided criteria • Ensure the success of the program through collaborative partnerships with patients, HCPs, field, and operational partners • Lead and facilitate weekly touchpoint meetings with field partners to review wins, priorities and action items; document outcomes and drive timely follow-through • Monitor and prioritize daily and weekly workload to anticipate needs, rebalance tasks, and ensure timely follow-through on commitments • Work and communicate cohesively within a team to identify collaborative opportunities, enable process improvement and escalate as needed • Provide manager and the account team voice of the customer feedback on the product, support, and insights to enable enhancements • Ensure all activities are conducted in a manner that complies with all Momentum, client, and industry-mandated rules and regulations. • Complete AEPQC reporting and provide all communications in a compliant manner.

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel is currently seeking a Clinical Trial Manager (CTM) to join us in the UK, dedicated to a single sponsor. This role will act as a member of the sponsor’s Development Operations team. The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group. Working as a Clinical Trial Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work. Expect exciting professional challenges in inspiring studies, but with time for your outside life. Responsibilities - Manage external vendors and contract research organisations. - Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual. - Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents. - Assist with protocol development and study report completion. - Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols. - Provide guidance, direction, and management to CRAs. - Track patient enrollment; qualify, initiate, monitor, perform closeout activities, and review site reports; and assist in coordination of data management activities. - Coordinate study supplies. - Negotiate contracts with vendors of clinical trial services. - Review Informed Consent Forms, CRFs, and study related materials. - Plan and participate in investigator meetings. - Assist and support data query process. - Assure regulatory compliance of investigational sites with sponsor’s SOPs and FDA and ICH guidelines. - Ensures trial master file is current and maintained. Please note that responsibilities may require a work schedule that may include working outside of “normal” work hours, to meet business demands. Here are a few requirements specific to this advertised role. - Bachelor’s, nursing degree or equivalent required, science preferred. - 5 or more years of industry experience in clinical studies (Pharmaceutical, Biotech or CRO). - Proven track record with relevant clinical trials experience, including strong performance as a CRA in the pharmaceutical industry (i.e. biotechnology, pharmaceutical, CRO, medical device). - Proven experience of clinical trial management. - Experience in CNS and / or oncology is preferred. - Proven management/leadership of people in a matrixed environment. - Management of global clinical trials. - Demonstrated working knowledge of GCP, ICH guidelines and FDA regulations. - Demonstrated ability to work independently and in a team environment. - Travel required. Must be willing to travel 15-25%, including international travel. - Proficiency with MS Office (e.g. Word, Excel, PowerPoint, Outlook). - Excellent oral and written communication skills and strong organisational abilities. We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel. Who are Parexel Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients. You’ll be an influential member of the wider team. Not quite the role for you? Join Our Talent Community and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events. Sign up today https://jobs.parexel.com/functional-service-provider

Core Responsibilities - Develop, maintain, and optimise detailed project schedules using recognised planning tools, Primavera P6 & Oracle Primavera Cloud - Build and manage integrated master schedules for large or multi‑workstream programmes. - Ensure logical sequencing of activities, dependencies, constraints, and milestones. - Conduct schedule health checks, critical path analysis, and performance measurement. - Support Planning Managers on projects underway - Develop and manage programmes from Pre-Construction, Construction & Commissioning to deliver various size data centres globally, inclusive of critical build sequencing, procurement and delivery of key plant & equipment, and ensuring clients have early access to the data halls while construction is still being completed and commissioning is underway. - Establish reporting cadence with GC’s and customers with a framework put in place to feed the relevant information into the required reporting platforms - Advise on a project-to-project basis on the correct and most suitable construction methods to use depending on timeframes and budgets. - Review standard architectural and engineering specifications to develop the programme and scheduling approach for each project. - Manage the coordinated interfaces with the Project and Design teams to ensure all work packages are developed timeously upfront to feed into the project schedules. - Develop and manage detailed schedules, inclusive of critical path analysis and ensuring programme logic is maintained through the project programme life. - Integrate multiple schedules into a master programme schedule, baselined with full critical path integration. - Additional programme development and management will include but not limited to customer RFP integrated master schedules for each development scheme, local council planning submissions, design schedules and procurement schedules for onboarding of critical consultants, contractors and ordering of key plant & equipment. - Work closely with various departments to ensure accurate delivery plans - Work closely with the customer scheduling teams to develop solid working relationships - Work closed with the GC and contractors teams to understand the schedules and extract the required information when needed to suit the reporting cadence