Senior Clinical Manager Job at Alexion Pharmaceuticals,Inc., Boston, MA

bEFVUThJMHI5VDRUdUhEL0hmYmZNUT09

Job Description

Some opportunities happen only once in a lifetime - like a job where you have the chance to change lives. At Alexion, people living with rare and devastating diseases are our Guiding Star. We are driven to continuously innovate and create meaningful value in all we do to help patients and families fully live their best lives. We value the uniqueness and diversity of our employees and recognize that nurturing the diverse perspectives and strengths of our people translates into innovative breakthroughs for patients.


This is what you will do:

Assist the CPLs for the planning, implementation, execution and compliance of operational plans for clinical study/program with multiple clinical vendors in order to maintain inspection readiness. This is a tactical position and involves protocol execution at the site level via established vendor oversight and escalation pathways. Serve as a peer mentor for staff, as needed. Ensure quality of the trial master file through content (QC) review of document packages submitted for entry into the TMF and liaise with the TMF specialist to resolve any issues identified with the documents submitted. Depending on the program scope, the CTM II may have study level responsibilities similar to any other CTM.


You will be responsible for:

  • Customizing/updating any study-specific plans and process flows for multiple clinical vendors, as appropriate e.g., site training plan, site monitoring plan, cross functional data review plan, IP release plan etc.
  • Assisting the CPL by tracking compliance to all study level plans and escalating any variances.
  • Serving as system expert and point of contact for business technologies used during the study (e.g., EDC, Investigator Portal, TMF).
  • Ensuring CRA compliance with the study parameters and track escalation and closure of action items noted in the monitoring visit reports (Late Phase studies only).
  • Ensuring registration of a protocol in ClinTrials.gov/EUdract and monitoring its update throughout a study’s life cycle for compliance with the regulations and SOP.
  • Assisting CPL with interactions with CRO and site staff to adhere to study budgets, requesting accruals, and performing contract and invoice review.
  • Participating in operation meetings with CRO, and cross-functional team members; documenting escalations and actions.
  • Coordinating study team training in the investigator portal; monitoring site/CRA user access and tracking compliance during the study.
  • Coordinating with CPL and cross-functional team to assemble study documents as appendices for CSR at study close-out.
  • Upon site closure, preparing subject files, inventories documents, reconciling document discrepancies, and organizing study files for electronic archive and off-site storage.
  • Serving as SME for initiatives in conjunction with the Center of Excellence, as required to ensure consistent implementation of best practices across all studies and within a franchise.

You will need to have:

  • Bachelor’s degree or equivalent in one of the disciplines related to clinical practice/health care, life sciences, or drug development
  • Excellent written and verbal skills and strong interpersonal skills
  • Proficiency in Microsoft Office Suite and email.
  • The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

We would prefer for you to have:

  • >3 years of clinical research experience/in the pharmaceutical industry with a solid understanding of technology and processes used in drug development.
  • Worked with CROs and vendors to drive timelines and deliverables.
  • Experience working with study budgets and forecasting; contract and invoice review.
  • Research certification desirable.

#LI-BP1

#LI-HYBRID


Alexion is a global biopharmaceutical company focused on serving patients and families affected by rare diseases and devastating conditions through the discovery, development and commercialization of life-changing medicines. Headquartered in Boston, Massachusetts, Alexion has offices around the globe and serves patients in more than 50 countries. Further information about Alexion can be found at: www.alexion.com.


Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion has taken critical steps to protect colleagues, loved ones, and patients from COVID-19 and its variants. All US-based employees must comply with Alexion's COVID-19 vaccination mandate. Alexion provides exceptions based on applicable state law as well as reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding a legally required exemption or accommodation, please contact accommodations@Alexion.com. Alexion participates in E-Verify.


As a leading employer in our industry, Alexion offers a highly competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness and financial security of our employees and their families. Benefits include group medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, and much more.


AstraZeneca completed its acquisition of Alexion, marking the creation of Alexion, AstraZeneca Rare Disease. If you're interested in career opportunities with AstraZeneca, click here.

Similar Jobs

Johnson & Johnson

Process Technician Job at Johnson & Johnson

Support foundry equipment and processes (Wax Injection presses, Shell, Pour & Finishing Equipment). Perform routine process testing and adjust the process

Expedite Solutions

Security Guard Job at Expedite Solutions

Shift Hours : 6AM-2PM , 2PM-10PM*. 10 PM to 6.00 AM*. Be at least twenty-one (21) years of age on the date of application; Customer service: 1 year (Preferred).

Marshalls

Customer Service Manager Job at Marshalls

Responsible for promoting an excellent customer experience. Oversees a team of Associates at front of store ensuring prompt, courteous customer service and

Easy Money

Store Manager Job at Easy Money

The successful candidate will be able to enhance customer satisfaction, meet sales and profitability goals and manage effectively.

The Mom Project

Assistant Bookkeeper Job at The Mom Project

We are looking for a bookkeeper on an ongoing basis to support a family office with a focus on real estate investment and hospitality management.